Bupropion Hydrochloride
- Product NDC
- 71610-899
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA206975
- Marketing category
- ANDA
- Substance
- BUPROPION HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-899-53 | 60 TABLET in 1 BOTTLE (71610-899-53) | 2025-04-15 | | No | Historical |
| 71610-899-60 | 90 TABLET in 1 BOTTLE (71610-899-60) | 2025-04-15 | | No | Historical |
| 71610-899-80 | 180 TABLET in 1 BOTTLE (71610-899-80) | 2025-04-15 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Bupropion Hydrochloride | Aphena Pharma Solutions - Tennessee, LLC | 2025-04-21 | HUMAN PRESCRIPTION DRUG LABEL | 1 |