NALTREXONE HYDROCHLORIDE
Active substance: naltrexone
TABLET, FILM COATED · NALTREXONE HYDROCHLORIDE 50 mg/1
United StatesActive
Marketing holder: Golden State Medical Supply, Inc.
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 3
- NALTREXONE HYDROCHLORIDE · 50 mg/1
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 14 |
|
| EU 1 |
|
Control by country
- 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
- Registration number
- 51407-959
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
- product · openFDA NDC · 51407-959 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 51407-959 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 51407-959 · Verified 2026-10-09 · open in source