Bupropion Hydrochloride
- Product NDC
- 50090-7322
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA216766
- Marketing category
- ANDA
- Substance
- BUPROPION HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7322-0 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7322-0) | 2024-10-15 | | No | Historical |
| 50090-7322-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7322-1) | 2024-10-15 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Bupropion Hydrochloride SR | A-S Medication Solutions | 2024-10-21 | HUMAN PRESCRIPTION DRUG LABEL | 2 |