Bosqichlar

Subyektlar

Tadbirlar

Ijro muddatlari

1-bosqich

Ariza beruvchi

Giyohvandlik vositalari va psixotrop moddalarni (keyingi oʻrinlarda — giyohvandlik vositalari) olib kirish, olib chiqishga sertifikat olish uchun kerak boʻladigan hujjatlarni tayyorlaydi va “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasiga (keyingi oʻrinlarda — Markaz) “Litsenziya” AT orqali yuboradi.

Ariza beruvchining xohishiga koʻra

2-bosqich

Markaz

1. Markaz sertifikatni rasmiylashtirish uchun kerakli hujjatlarni ariza beruvchidan qabul qilib olganidan soʻng boshqa vakolatli organlardan quyidagi hujjatlar va maʼlumotlarni oʻzaro axborot hamkorligi orqali elektron shaklda oladi:

a) dori vositasi tarkibida giyohvandlik vositalari mavjud boʻlgan hollarda, ushbu dori vositasi uchun berilgan roʻyxatdan oʻtkazish guvohnomasining nusxasi;

b) Sogʻliqni saqlash vazirligi tomonidan berilgan giyohvandlik vositalari muomalasi bilan bogʻliq faoliyatni amalga oshirish huquqini beruvchi litsenziyaning nusxasi.

2. Markaz hujjatlar toʻplamini oʻrganadi va kelishish uchun “Litsenziya” AT orqali DXX hamda IIVga yuboradi.

1-2. Ariza va hujjatlar qabul qilingan kunda

3. DXX va IIV hujjatlarni koʻrib chiqib, tegishli xulosasini Agentlikka yuboradi.

3. Hujjatlar qabul qilingandan soʻng yigirma ish kunidan ortiq boʻlmagan muddatda

4. Agentlik hujjatlarni koʻrib chiqib, tegishli qarorni Markazga taqdim etadi.

4. Hujjatlar qabul qilingandan soʻng besh ish kunidan ortiq boʻlmagan muddatda

5. Agentlik qarori asosida Markaz ariza beruvchiga sertifikat berilishi toʻgʻrisida yoki DXX va IIVning (rad etilgan holatda) tegishli xulosalari asosida rad etish asoslari va qonunchilikning aniq normalarini koʻrsatgan holda ariza beruvchiga “Litsenziya” AT orqali xabarnoma yuboradi.

6. Markaz sertifikatni anʼanaviy tarzda ariza beruvchining oʻziga yoki pochta xizmati orqali ariza beruvchi koʻrsatgan manzilga yuboradi.

5-6. Tegishli qaror olingandan soʻng besh ish kundan ortiq boʻlmagan muddatda

3-bosqich

(zarur boʻlganda)

Markaz

Ariza beruvchi sertifikat berishni rad etish uchun asos boʻlgan sabablarni bartaraf etgan hollarda, sertifikat berish uchun hujjatlarni qayta koʻrib chiqadi yoki sertifikat berishni rad etadi.

Ariza va hujjatlar qabul qilingandan soʻng oʻn ish kundan ortiq boʻlmagan muddatda

OʻZBEKISTON RESPUBLIKASI SOGʻLIQNI SAQLASH VAZIRLIGINING

“FARMATSEVTIKA MAHSULOTLARI XAVFSIZLIGI MARKAZI” DAVLAT MUASSASASI

GIYOHVANDLIK VOSITALARINI OLIB KIRISH UCHUN

__________-SON SERTIFIKAT

(boshqa yuridik shaxsga bermaslik sharti bilan, nusxalari haqiqiy emas)

Birlashgan Millatlar Tashkilotining 1961-yildagi Giyohvandlik vositalari toʻgʻrisidagi yagona konvensiyasida nazarda tutilgan giyohvandlik vositalari va ularning hosilalari haqidagi tegishli qonunlarni qoʻllash uchun masʼul boʻlgan “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasi:

_________________________________________________________________________________________

^{(import qiluvchi tashkilot nomi va uning manzili)}

_________________________________________________________________________________________

_______________________________________________________________________________________ga

Oʻzbekiston Respublikasiga _______________________________________________________________

^{(eksport qiluvchi tashkilot nomi va uning manzili)}

______________________________________________________________________________________dan

quyidagi giyohvandlik vositalarini (xalqaro patentlanmagan nomi, dori shakli, dozasi, miqdori):

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

olib kelishga ruxsat etadi.

Sertifikatda koʻrsatilgan giyohvandlik vositalari:

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

__________________________________________________________ maqsadlari uchun foydalaniladi.

Mazkur sertifikatning amal qilish muddati

20___ y. “___” __________

Markaz direktori

20___ y. “____” __________

(orqa tomoni)

STATE INSTITUTION “CENTER FOR PHARMACEUTICAL PRODUCTS SAFETY”

OF THE MINISTRY OF HEALTH OF THE REPUBLIC OF UZBEKISTAN

CERTIFICATE № __________

on the import of narcotics

(provided that it is not given to another legal entity, the copy is not authentic)

This is to certify that State institution “Centre for pharmaceutical products safety” entrusted with the application of laws on narcotics and their derivatives envisaged by 1961 UN Single Convention on Narcotics permits:

_________________________________________________________________________________________

^{(name and address importer)}

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

to import in Republic of Uzbekistan from

_________________________________________________________________________________________

^{(name and address exporter)}

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

undermentioned narcotics (international nonproprietary name, pharmaceutical name, dosage, number):

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

Above-stated narcotics are to be used in:

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

The certificate is valid up to

_____________ “____”, 20____

Director of the center

________________ “____”, 20____.

OʻZBEKISTON RESPUBLIKASI SOGʻLIQNI SAQLASH VAZIRLIGINING

“FARMATSEVTIKA MAHSULOTLARI XAVFSIZLIGI MARKAZI” DAVLAT MUASSASASI

PSIXOTROP MODDALARNI OLIB KIRISH UCHUN

__________-SON SERTIFIKAT

(boshqa yuridik shaxsga bermaslik sharti bilan, nusxalari haqiqiy emas)

Birlashgan Millatlar Tashkilotining 1971-yildagi Psixotrop moddalar toʻgʻrisidagi konvensiyasida nazarda tutilgan psixotrop moddalar va ularning hosilalari toʻgʻrisidagi tegishli qonunlarni qoʻllash uchun masʼul boʻlgan “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasi:

_________________________________________________________________________________________

^{(import qiluvchi tashkilot nomi va uning manzili)}

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

_______________________________________________________________________________________ga

Oʻzbekiston Respublikasiga ________________________________________________________________

^{(import qiluvchi tashkilot nomi va uning manzili)}

_____________________________________________________________________________________dan

psixotrop moddalar saqlagan quyidagi dori vositalarini (xalqaro patentlanmagan nomi, dori shakli, dozasi, miqdori):

_________________________________________________________________________________________

_________________________________________________________________________________________

olib kelishga ruxsat etadi.

Sertifikatda koʻrsatilgan psixotrop moddalar:

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

____________________________________________________________ maqsadlari uchun foydalaniladi.

Mazkur sertifikatning amal qilish muddati

20___ y. “____” ___________

Markaz direktori

20____ y. “____” __________

(orqa tomoni)

STATE INSTITUTION “CENTER FOR PHARMACEUTICAL PRODUCTS SAFETY”

OF THE MINISTRY OF HEALTH OF THE REPUBLIC OF UZBEKISTAN

CERTIFICATE № __________

on the import of psychotropic agents

(provided that it is not given to another legal entity, the copy is not authentic)

This is to certify that State institution “Centre for pharmaceutical products safety” entrusted with the application of laws on psychotropic agents and their derivatives envisaged by 1971 UN Convention on psychotropic agents permits:

_________________________________________________________________________________________

^{(name and address of importer)}

_________________________________________________________________________________________

_________________________________________________________________________________________

to import in Republic of Uzbekistan from

_________________________________________________________________________________________

^{(name and address of exporter)}

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

under mentioned psychotropic agents (international nonproprietary name, pharmaceutical form, dosage, number):

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

Above-stated psychotropic agents will be used in:

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

The certificate is valid up to

_____________ “____”, 20___

Director of the center

_____________ “____”, 20___

OʻZBEKISTON RESPUBLIKASI SOGʻLIQNI SAQLASH VAZIRLIGINING

“FARMATSEVTIKA MAHSULOTLARI XAVFSIZLIGI MARKAZI” DAVLAT MUASSASASI

GIYOHVANDLIK VOSITALARINI OLIB CHIQISH UCHUN

__________-SON SERTIFIKAT

(boshqa yuridik shaxsga bermaslik sharti bilan, nusxalari haqiqiy emas)

Birlashgan Millatlar Tashkilotining 1961-yildagi Giyohvandlik vositalari toʻgʻrisidagi yagona konvensiyasida nazarda tutilgan giyohvandlik vositalari va ularning hosilalari toʻgʻrisidagi tegishli qonunlarni qoʻllash uchun masʼul boʻlgan “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasi:

_________________________________________________________________________________________

^{(eksport qiluvchi tashkilot nomi va uning manzili)}

_________________________________________________________________________________________

_________________________________________________________________________________________

______________________________________________________________________________________dan

Oʻzbekiston Respublikasidan _______________________________________________________________

^{(import qiluvchi tashkilot nomi va uning manzili)}

_______________________________________________________________________________________ga

quyidagi giyohvandlik vositalarini (xalqaro patentlanmagan nomi, dori shakli, dozasi, miqdori):

_________________________________________________________________________________________

_________________________________________________________________________________________

import qiluvchi mamlakatning import ruxsatnomasi asosida (berilgan sanasi)

_________________________________________________________________________________________

olib chiqilishiga ruxsat etadi.

Sertifikatda koʻrsatilgan giyohvandlik vositalari: ____________________________________________

____________________________________________________________ maqsadlari uchun foydalaniladi.

Mazkur sertifikatning amal qilish muddati

20____ y. “____” ___________

Markaz direktori

20___ y. “___” __________

(orqa tomoni)

STATE INSTITUTION “CENTER FOR PHARMACEUTICAL PRODUCTS SAFETY”

OF THE MINISTRY OF HEALTH OF THE REPUBLIC OF UZBEKISTAN

CERTIFICATE № __________

on the export of narcotics

(provided that it is not given to another legal entity, the copy is not authentic)

This is to certify that State institution “Centre for pharmaceutical products safety” entrusted with the application of laws on narcotics and their derivatives envisaged by 1961 UN Single Convention on narcotics permits:

_________________________________________________________________________________________

^{(name and address exporter)}

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

to export from the Republic of Uzbekistan in

_________________________________________________________________________________________

^{(name and address of importer)}

_________________________________________________________________________________________

_________________________________________________________________________________________

under mentioned narcotics (international nonproprietary name, pharmaceutical name, dosage, number):

_________________________________________________________________________________________

authorization to import of the importer country (date of issue)

_________________________________________________________________________________________

_________________________________________________________________________________________

Above-stated narcotics will be used in:

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

The certificate is valid up to

_____________ “____”, 20___

Director of the center

_____________ “____”, 20___

OʻZBEKISTON RESPUBLIKASI SOGʻLIQNI SAQLASH VAZIRLIGINING

“FARMATSEVTIKA MAHSULOTLARI XAVFSIZLIGI MARKAZI” DAVLAT MUASSASASI

PSIXOTROP MODDALARNI OLIB CHIQISH UCHUN

__________-SON SERTIFIKAT

(boshqa yuridik shaxsga bermaslik sharti bilan, nusxalari haqiqiy emas)

Birlashgan Millatlar Tashkilotining 1971-yildagi Psixotrop moddalar toʻgʻrisidagi konvensiyasida nazarda tutilgan psixotrop moddalar va ularning hosilalari haqidagi tegishli qonunlarni qoʻllash uchun masʼul boʻlgan “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasi:

_________________________________________________________________________________________

^{(eksport qiluvchi tashkilot nomi va uning manzili)}

_________________________________________________________________________________________

______________________________________________________________________________________dan

Oʻzbekiston Respublikasidan _______________________________________________________________

^{(import qiluvchi tashkilot nomi va uning manzili)}

psixotrop moddalar saqlagan quyidagi dori vositalarini (xalqaro patentlanmagan nomi, dori shakli, dozasi, miqdori):

_________________________________________________________________________________________

import qiluvchi mamlakatning import ruxsatnomasi asosida (berilgan sanasi)

_________________________________________________________________________________________

olib chiqilishiga ruxsat etadi.

Sertifikatda koʻrsatilgan psixotrop moddalar: _______________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

___________________________________________________________ maqsadlari uchun foydalaniladi.

Mazkur sertifikatning amal qilish muddati

20____ y. “____” __________

Markaz direktori

20____ y. “____” __________

(orqa tomoni)

STATE INSTITUTION “CENTER FOR PHARMACEUTICAL PRODUCTS SAFETY”

OF THE MINISTRY OF HEALTH OF THE REPUBLIC OF UZBEKISTAN

CERTIFICATE № __________

on the export of psychotropic agents

(provided that it is not given to another legal entity, the copy is not authentic)

This is to certify that State institution “Centre for pharmaceutical products safety” entrusted with the application of laws on psychotropic agents and their derivatives envisaged by 1971 UN Convention on psychotropic agents permits:

_________________________________________________________________________________________

^{(name and address of exporter)}

_________________________________________________________________________________________

_________________________________________________________________________________________

_________________________________________________________________________________________

to export from Republic of Uzbekistan in

_________________________________________________________________________________________

^{(name and address of importer)}

under mentioned medicines containing psychotropic agents (international nonproprietary name, pharmaceutical name, dosage, number):

_________________________________________________________________________________________

_________________________________________________________________________________________

authorization to import of the importer country (date of issue)

_________________________________________________________________________________________

_________________________________________________________________________________________

Above-stated psychotropic agents will be used in:

_________________________________________________________________________________________

_________________________________________________________________________________________

The certificate is valid up to

_____________ “___”, 20___

Director of the center

_____________ “___”, 20___

Oʻzbekiston Respublikasi Sogʻliqni saqlash vazirligining “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasiga

Ushbu bilan ______________________________________________________________________________

_________________________________________________________________________________________

^{(ariza beruvchi nomi, STIR, mamlakat nomi, yuridik manzili, tel./faks koʻrsatilgan holda)}

Sizdan olib kelinayotgan (olib chiqilayotgan) __________________________________________________

^{(giyohvandlik vositalari va psixotrop moddalarning}

_______________________________________________________________________________________ni

^{xalqaro patentlanmagan nomini koʻrsatgan holda dori shakli, dozasi, miqdori)}

_________________________________________________________________________________________

^{(kontrakt (shartnoma) raqami va sanasi, ishlab chiqaruvchi nomi,}

_________________________________________________________________________________________

^{yuk joʻnatuvchi, yuk yetkazib beruvchi nomi, mamlakati, yuridik manzili, tel./faks)}

asosida olib kirish (olib chiqish) sertifikatini berishingizni soʻraymiz.

Olib kelinayotgan (olib chiqilayotgan) ________________________________________ uchun ishlatiladi.

^{(giyohvandlik vositalari va psixotrop moddalarning foydalanish maqsadi)}

Yuk _____________________________________________________________________________________

^{(yoʻnalish, transport turi, eksport qiluvchi mamlakatdan import qiluvchi mamlakatga}

_________________________________________________________________________________________

^{chiqish-kirish nuqtalarini koʻrsatgan marshruti bilan)}

_________________________________________________________________________________________

^{(moʻljallangan olib kirish, olib chiqish muddati)}

____________________________________________________________________________ olib kelinadi.

^{(yetkazib berish tartibi (bir partiyada))}

Shu bilan birga, import qilinadigan mahsulotlarni reeksport qilmaslik majburiyatini olamiz.

Masʼul shaxs F.I.O. va imzosi

M.Oʻ.

Oʻzbekiston Respublikasi Sogʻliqni saqlash vazirligining “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasiga

Ushbu bilan ______________________________________________________________________________

_________________________________________________________________________________________

^{(ariza beruvchi nomi, STIR, mamlakat nomi, yuridik manzili, tel./faks koʻrsatilgan holda)}

Sizdan __________________________________________________________________________________

^{(giyohvandlik vositalari va psixotrop moddalarning}

_________________________________________________________________________________________

^{xalqaro patentlanmagan nomini koʻrsatgan holda dori shakli, dozasi, miqdori)}

________________________________________________________________________________________

^{(ishlab chiqaruvchi nomi, yuk joʻnatuvchi, yuk yetkazib beruvchi nomi, mamlakati, yuridik manzili, tel./faks)}

______________________________________________________________ insonparvarlik yordami yukini

olib kirish (olib chiqish) ruxsatnomasini berishingizni soʻraymiz.

Olib kelinayotgan (olib chiqilayotgan) insonparvarlik yordami yukidan ____________________________

______________________________________________________________________ uchun foydalaniladi.

^{(foydalanish maqsadi)}

Yuk ________________________________________________________________________ olib kelinadi

^{(transport turi)}

Masʼul shaxs F.I.O. va imzosi

M.Oʻ.

INSONPARVARLIK YORDAMI YUKLARINI OLIB KIRISH/OLIB CHIQISH UCHUN

_____-SON RUXSATNOMA

Sogʻliqni saqlash vazirligining “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasi ruxsat etadi:

_________________________________________________________________________________________

^{(import qiluvchi tashkilot nomi va manzili)}

_______________________________________________________________________________________ga

Oʻzbekiston Respublikasiga _________________________________________________________________

^{(eksport qiluvchi tashkilot nomi va manzili)}

_________________________________________________________________________________________

tashkilotidan quyidagi dori vositalari olib kelinadi:

_________________________________________________________________________________________

^{(xalqaro patentlanmagan nomi, dori shakli, dozasi, miqdori)}

_________________________________________________________________________________________

_________________________________________________________________________________________

Ushbu dori vositalaridan __________________________________________________________________

_______________________________________________________________ maqsadlarida foydalaniladi.

* giyohvandlik vositalari va psixotrop moddalardan laboratoriyaning ijobiy xulosasi olingandan soʻng foydalanilishiga ruxsat etiladi.

Markaz direktori

20____ y. “____” ______________

Bosqichlar

Subyektlar

Tadbirlar

Ijro muddatlari

1-bosqich

Ariza beruvchi

Giyohvandlik vositalari va psixotrop moddalarni (keyingi oʻrinlarda — giyohvandlik vositalari) Oʻzbekiston Respublikasi hududi orqali tranzit tarzida oʻtkazishga ruxsatnoma olish uchun kerak boʻladigan hujjatlarni tayyorlaydi va “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasiga (keyingi oʻrinlarda — Markaz) “Litsenziya” AT orqali yuboradi.

Ariza beruvchining xohishiga koʻra

2-bosqich

Markaz

1. Markaz hujjatlar toʻplamini oʻrganadi, kelishish uchun “Litsenziya” AT orqali DXX hamda IIVga yuboradi.

1. Ariza va hujjatlar qabul qilingan kunda

2. DXX va IIV hujjatlarni koʻrib chiqib, tegishli xulosasini Agentlikka yuboradi.

2. Hujjat qabul qilingandan soʻng oʻn ish kunidan ortiq boʻlmagan muddatda

3. Agentlik hujjatlarni koʻrib chiqib, tegishli qarorni Markazga taqdim etadi.

3. Hujjat qabul qilingandan soʻng besh ish kunidan ortiq boʻlmagan muddatda

4. Agentlik qarori asosida Markaz ariza beruvchiga ruxsatnoma berilishi toʻgʻrisida yoki DXX va IIVning (rad etilgan holatda) tegishli xulosalari asosida rad etish asoslari va qonunchilikning aniq normalarini koʻrsatgan holda ariza beruvchiga “Litsenziya” AT orqali xabarnoma yuboradi.

5. Markaz ruxsatnomani anʼanaviy tarzda ariza beruvchining oʻziga yoki pochta xizmati orqali ariza beruvchi koʻrsatgan manzilga yuboradi.

4-5. Tegishli qaror olingandan soʻng besh ish kundan ortiq boʻlmagan muddatda

3-bosqich

(zarur boʻlganda)

Markaz

Ariza beruvchi tranzit ruxsatnomasini berishni rad etish uchun asos boʻlgan sabablarni bartaraf etgan hollarda, hujjatlarni qayta koʻrib chiqadi, tranzit ruxsatnomasini beradi yoki berishni rad etadi.

Ariza va hujjatlar qabul qilingandan soʻng besh ish kundan ortiq boʻlmagan muddatda

OʻZBEKISTON RESPUBLIKASI SOGʻLIQNI SAQLASH VAZIRLIGINING

“FARMATSEVTIKA MAHSULOTLARI XAVFSIZLIGI MARKAZI” DAVLAT MUASSASASI

Giyohvandlik vositalari va psixotrop moddalarni Oʻzbekiston Respublikasi hududi orqali tranzit tarzida oʻtkazishga

-SON RUXSATNOMA

“Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasi berilgan arizani koʻrib chiqib,

______________________________________________________________________________________ ga

^{(tashkilot nomi va uning manzili)}

________________________________________________________________________________________

quyidagi miqdordagi _____________________________________________________________________

^{(giyohvandlik vositalari va psixotrop moddalar nomi)}

________________________________________________________________________________________

^{(ogʻirligi, hajmi, dori shakli, dozasi, qutilar soni)}

____________________________________________________________ tranzit qilinishiga ruxsat etadi.

Yukning yoʻnalishi, marshruti, transport turi:

________________________________________________________________________________________

Mazkur ruxsatnomaning amal qilish muddati 20____ y. “______” __________

Markaz direktori

Berilgan sana 20____ y. “______” __________

Oʻzbekiston Respublikasi Sogʻliqni saqlash vazirligining “Farmatsevtika mahsulotlari xavfsizligi markazi” davlat muassasasiga

Ushbu bilan ______________________________________________________________________________

_______________________________________________________________________________________ga

^{(importyor qiluvchi tashkilot, yuk joʻnatuvchi va mamlakat nomi, yuridik manzili)}

Sizdan __________________________________________________________________________________

^{(giyohvandlik vositalari va psixotrop moddalarning}

____________________________________________________________________________________ uchun

^{xalqaro patentlanmagan nomini koʻrsatgan holda dori shakli, dozasi, miqdori)}

________________________________________________________________________________________

^{(kontrakt (shartnoma) raqami va sanasi, yuk joʻnatuvchi,}

________________________________________________________________________________________

^{yuk yetkazib beruvchi nomi, mamlakati, yuridik manzili)}

asosida tranzit ruxsatnomasini olishga ruxsat berishingizni soʻraymiz.

______________________________________________________________________ uchun foydalaniladi.

^{(foydalanish maqsadi)}

________________________________________________________________________________________

^{(yoʻnalish, transport turi, eksport qiluvchi mamlakatdan import qiluvchi mamlakatga}

________________________________________________________________________________________

^{chiqish-kirish nuqtalarini koʻrsatgan marshruti bilan)}

________________________________________________________________________________________

^{(moʻljallangan olib kirish, olib chiqish muddati)}

________________________________________________________________________________________

^{(yetkazib berish tartibi (bir partiyada))}

Masʼul shaxs F.I.O. va imzosi

M.Oʻ.

1.

Morfin

0,5

2.

Trimeperidin

5,0

3.

Kodein + Morfin + Noskapin + Papaverin + Tebain

0,1

4.

Buprenorfin, Buprenorfin + Nalokson

0,13

5.

Kodein

70,3

6.

Fentanil

0,04

T/r

Boʻlim nomi

Giyohvandlik vositalari nomi

Morfin gidroxlorid 1%-1,0

Omnopon 1%-1,0

Omnopon 2%-1,0

Promedol 1%-1,0

Promedol 2%-1,0

Quruq morfinsimon preparatlar yigʻindisi

Fentanil 0,005 %-2,0

Promedol kukuni

Promedol tabletkasi

Etilmorfin gidroxlorid

(sof modda)

Kodein, uning tuzlari

Tarkibida yoʻtalga qarshi kodein bor boʻlgan tabletkalar

Buprenorfin 0,3 mg

Buprenorfin 0,6 mg

Fortral (Pentazo-sin)

Oʻlchov birligi

Amp.

Amp.

Amp.

Amp.

Amp.

Amp.

Amp.

Gr.

Qad.

Gr.

Gr.

Qad.

Amp.

Amp.

Amp.

1.

Terapevtik

3,0

0,5

2,0

0,5

5,0

11,0

0,4

0,25

1,5

0,5

0,2

5,0

—

—

0,5

2.

Gastroenterologik

3,0

—

0,5

0,5

5,5

9,5

1,0

—

0,5

-

—

2,0

—

—

0,5

3.

Kardiologik

1,0

0,5

1,5

0,5

5,5

9,0

1,5

—

1,0

2,0

—

1,0

—

—

0,5

4.

Pulmonologik

1,0

1,0

2,0

1,0

6,0

11,0

0,5

—

—

0,06

0,2

4,0

—

—

1,0

5.

Allergologik

—

—

—

—

1,0

1,0

—

—

—

-

—

1,0

—

—

—

6.

Endokrinologik

—

—

0,6

—

1,0

1,6

3,0

—

—

0,01

—

0,1

—

—

—

7.

Nefrologik

6,0

2,0

7,0

0,5

55,0

75,0

6,0

—

—

-

—

1,5

—

—

—

8.

Revmatologik

2,5

2,0

12,0

4,0

36,0

56,5

5,0

—

0,5

0,3

—

1,5

—

—

4,0

9.

Profpatologik

1,0

1,0

2,0

0,5

6,0

10,5

—

—

—

0,06

0,2

3,0

—

—

0,05

10.

Jarrohlik

6,0

1,5

8,5

7,0

58,0

81,0

6,0

0,4

10,0

0,4

0,3

6,0

3,0

3,0

7,0

11.

Travmatologik

8,0

1,0

4,0

10,0

100,0

—

10,0

—

—

0,5

—

2,0

—

—

2,0

12.

Ortopedik

—

—