BUPROPION HYDROCHLORIDE
Active substance: Bupropion
TABLET, EXTENDED RELEASE · BUPROPION HYDROCHLORIDE 150 mg/1
United StatesActive
Marketing holder: REMEDYREPACK INC.
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
Composition
- BUPROPION HYDROCHLORIDE · 150 mg/1
Analogues by country
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| EU 1 |
|
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-273b-7bad-8eff-8a7560f1e9c0,01a1208c-2752-724b-8f94-0f16aa40c3a4,01a1208c-29db-7d45-b421-b9aa063fde8b,01a1208c-2cfe-72dd-9a88-34a9c272d0ab,01a1208c-328f-775e-9927-8c2eeaac0396;count=347 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 70518-2458
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 70518-2458 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 70518-2458 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 70518-2458 · Verified 2026-10-09 · open in source