bupropion Hydrochloride
- Product NDC
- 72162-2400
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206975
- Marketing category
- ANDA
- Substance
- BUPROPION HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-2400-1 | 100 TABLET in 1 BOTTLE (72162-2400-1) | 2024-10-02 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| bupropion Hydrochloride | Bryant Ranch Prepack | 2025-01-06 | HUMAN PRESCRIPTION DRUG LABEL | 101 |