Bupropion Hydrochloride
- Product NDC
- 50090-7334
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207479
- Marketing category
- ANDA
- Substance
- BUPROPION HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7334-0 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7334-0) | 2024-10-15 | | No | Historical |
| 50090-7334-1 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7334-1) | 2024-10-15 | | No | Historical |