Bupropion Hydrochloride
- Product NDC
- 71205-967
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA210081
- Marketing category
- ANDA
- Substance
- BUPROPION HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-967-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-967-30) | 2020-06-09 | | No | Historical |
| 71205-967-55 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-967-55) | 2020-06-09 | | No | Historical |
| 71205-967-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-967-90) | 2020-06-09 | | No | Historical |