NDC 71335-0877 – bupropion Hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet · Oral
Product NDC71335-0877
Product details
- Brand name
- bupropion Hydrochloride
- Generic name
- bupropion Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207389
- Marketed since
- May 26, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for bupropion hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0877-1 | 60 TABLET in 1 BOTTLE (71335-0877-1) | Sep 7, 2018 |
| 71335-0877-2 | 30 TABLET in 1 BOTTLE (71335-0877-2) | Jun 21, 2018 |
| 71335-0877-3 | 100 TABLET in 1 BOTTLE (71335-0877-3) | Dec 27, 2021 |
| 71335-0877-4 | 90 TABLET in 1 BOTTLE (71335-0877-4) | Sep 13, 2018 |
| 71335-0877-5 | 120 TABLET in 1 BOTTLE (71335-0877-5) | Dec 27, 2021 |
| 71335-0877-6 | 15 TABLET in 1 BOTTLE (71335-0877-6) | Dec 27, 2021 |
| 71335-0877-7 | 21 TABLET in 1 BOTTLE (71335-0877-7) | Dec 27, 2021 |
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