Bupropion Hydrochloride
- Product NDC
- 50090-7112
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210015
- Marketing category
- ANDA
- Substance
- BUPROPION HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7112-0 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-7112-0) | 2024-03-11 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Bupropion Hydrochloride XL | A-S Medication Solutions | 2024-03-13 | HUMAN PRESCRIPTION DRUG LABEL | 4 |