Bupropion Hydrochloride
- Product NDC
- 50090-6872
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA205794
- Marketing category
- ANDA
- Substance
- BUPROPION HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-6872-0 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6872-0) | 2023-12-04 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Bupropion Hydrochloride SR | A-S Medication Solutions | 2024-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 4 |