Налтрексона гидрохлорид

Active substance: naltrexone

субстанция-порошок, ~, 0.1 -10 кг (original in Russian, GRLS)

RussiaActive

Marketing holder: Аспен Осс Б.В.

Verified 2026-10-09 · GRLS (Russian state register)

Composition

Analogues by country

Products with the same active substance registered in other countries.

Country	Products
US 49	Contrave Extended-Release TABLET, EXTENDED RELEASE · NALTREXONE HYDROCHLORIDE 8 mg/1, BUPROPION HYDROCHLORIDE 90 mg/1 51267-890 Nalpropion Pharmaceuticals LLC NALTREXONE HYDROCHLORIDE TABLET, FILM COATED · NALTREXONE HYDROCHLORIDE 50 mg/1 51407-959 Golden State Medical Supply, Inc. NALTREXONE HYDROCHLORIDE TABLET, FILM COATED · NALTREXONE HYDROCHLORIDE 50 mg/1 0904-7036 Major Pharmaceuticals NALTREXONE HYDROCHLORIDE TABLET, FILM COATED · NALTREXONE HYDROCHLORIDE 50 mg/1 70518-2718 REMEDYREPACK INC. NALTREXONE HYDROCHLORIDE TABLET, FILM COATED · NALTREXONE HYDROCHLORIDE 50 mg/1 0406-1170 SpecGx LLC All products in this country (49)
EU 1	Mysimba bupropion hydrochloride, naltrexone hydrochloride EMEA/H/C/003687 Orexigen Therapeutics Ireland Limited

Country

Products

US 49

Contrave Extended-Release
TABLET, EXTENDED RELEASE · NALTREXONE HYDROCHLORIDE 8 mg/1, BUPROPION HYDROCHLORIDE 90 mg/1
51267-890
Nalpropion Pharmaceuticals LLC
NALTREXONE HYDROCHLORIDE
TABLET, FILM COATED · NALTREXONE HYDROCHLORIDE 50 mg/1
51407-959
Golden State Medical Supply, Inc.
NALTREXONE HYDROCHLORIDE
TABLET, FILM COATED · NALTREXONE HYDROCHLORIDE 50 mg/1
0904-7036
Major Pharmaceuticals
NALTREXONE HYDROCHLORIDE
TABLET, FILM COATED · NALTREXONE HYDROCHLORIDE 50 mg/1
70518-2718
REMEDYREPACK INC.
NALTREXONE HYDROCHLORIDE
TABLET, FILM COATED · NALTREXONE HYDROCHLORIDE 50 mg/1
0406-1170
SpecGx LLC

EU 1

Mysimba
bupropion hydrochloride, naltrexone hydrochloride
EMEA/H/C/003687
Orexigen Therapeutics Ireland Limited

Import and control

Russiaprescription only
Source: GRLS (Russian state register) · record 01a120c3-a69a-70e6-848c-f3830f8566ec,01a120c3-a8d5-7d79-aa79-0b0173e04ad6,01a120c3-c96c-7da8-877a-0c3b2d7f02f4,01a120c4-0148-75a3-ac92-2890498811ff,01a120c4-c879-7793-8a58-525db823ef9e;count=9 · valid from 2026-10-09 · verified 2026-10-09
United Statesprescription only
Source: openFDA NDC · record 01a1208c-6f56-7717-9b31-eb7d65c1b9b2,01a1208c-990d-714f-abd8-45ccc8401376,01a1208c-9c88-7a6d-baa4-53868dd87e4a,01a1208c-9ef8-75f3-9bc5-6b0d3da9cc8c,01a1208c-a596-70ab-9007-f40424375869;count=48 · valid from 2026-10-09 · verified 2026-10-09