NDC 71335-2652 – Bupropion Hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2652
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075491
- Marketed since
- April 25, 2024
- 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 |
|---|---|---|
| 71335-2652-1 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2652-1) | Jun 3, 2025 |
| 71335-2652-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2652-2) | Jun 3, 2025 |
| 71335-2652-3 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2652-3) | Jun 3, 2025 |
| 71335-2652-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2652-4) | Jun 3, 2025 |
| 71335-2652-5 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2652-5) | Jun 3, 2025 |
| 71335-2652-6 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-2652-6) | Jun 3, 2025 |
| 71335-2652-7 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-2652-7) | Jun 3, 2025 |
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