AZATHIOPRINE
Active substance: azathioprine
TABLET · AZATHIOPRINE 50 mg/1
United StatesActive
Marketing holder: PD-Rx Pharmaceuticals, Inc.
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 3
- AZATHIOPRINE · 50 mg/1
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 6 |
|
| EU 1 |
|
Control by country
- Russiaprescription only
Source: GRLS (Russian state register) · record 01a120c3-744b-794a-88b7-028d5dc5d1ae,01a120c3-84ee-739f-a466-c5a19d635341,01a120c3-b555-7173-a932-c51067c5b64b,01a120c6-031d-7cb6-8d34-bfd4bf3e3fa3,01a120c6-affa-73e6-bab8-6f0189bee27b;count=5 · valid from 2026-10-09 · verified 2026-10-09
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-991b-702e-8b1b-227066f7c98a,01a1208c-bc52-7c53-b7b9-1db37db3342b,01a1208d-552d-75f1-b154-b42efe8bf83d,01a1208d-83a8-7e86-b1ac-b761e4cec724,01a1208d-87ea-7715-8010-e80adcc671f6;count=34 · valid from 2026-10-09 · verified 2026-10-09
- Registration number
- 72789-129
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
- product · openFDA NDC · 72789-129 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 72789-129 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 72789-129 · Verified 2026-10-09 · open in source