NDC 71335-0013 – Bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0013
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076143
- Marketed since
- January 17, 2006
- 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 |
|---|---|---|
| 71335-0013-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0013-1) | Mar 8, 2018 |
| 71335-0013-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0013-2) | Feb 21, 2018 |
| 71335-0013-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0013-3) | Jul 9, 2024 |
| 71335-0013-4 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-0013-4) | Jul 9, 2024 |
| 71335-0013-5 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0013-5) | Jul 9, 2024 |
| 71335-0013-6 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0013-6) | Jul 9, 2024 |
| 71335-0013-7 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0013-7) | Jul 9, 2024 |
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