NDC 71335-0791 – bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet · Oral
Product NDC71335-0791
Product details
- Brand name
- bupropion Hydrochloride
- Generic name
- bupropion Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA206975
- Marketed since
- August 19, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 75 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0791-1 | 30 TABLET in 1 BOTTLE (71335-0791-1) | Apr 26, 2018 |
| 71335-0791-2 | 60 TABLET in 1 BOTTLE (71335-0791-2) | Jun 19, 2019 |
| 71335-0791-3 | 90 TABLET in 1 BOTTLE (71335-0791-3) | Jun 19, 2019 |
| 71335-0791-4 | 7 TABLET in 1 BOTTLE (71335-0791-4) | Jun 19, 2019 |
| 71335-0791-5 | 14 TABLET in 1 BOTTLE (71335-0791-5) | Jun 19, 2019 |
| 71335-0791-6 | 120 TABLET in 1 BOTTLE (71335-0791-6) | Jun 19, 2019 |
| 71335-0791-7 | 100 TABLET in 1 BOTTLE (71335-0791-7) | Jun 19, 2019 |
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