Bupropion Hydrochloride
- Product NDC
- 68071-3559
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090693
- Marketing category
- ANDA
- Substance
- BUPROPION HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3559-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3559-9) | 2024-01-09 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Bupropion Hydrochloride | NuCare Pharmaceuticals,Inc. | 2025-01-03 | HUMAN PRESCRIPTION DRUG LABEL | 2 |