NDC 71335-0182 – Bupropion Hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0182
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 100 mg/1
Uses, dosage, side effects and warnings for bupropion hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0182-1 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0182-1) | Jul 24, 2018 |
| 71335-0182-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0182-2) | Jun 20, 2018 |
| 71335-0182-3 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3) | Jul 9, 2024 |
| 71335-0182-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4) | Mar 28, 2018 |
| 71335-0182-5 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0182-5) | Jul 9, 2024 |
| 71335-0182-6 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0182-6) | Jul 9, 2024 |
| 71335-0182-7 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-0182-7) | Apr 28, 2021 |
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