NDC 71335-0135 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71335-0135
Product details
- Brand name
- Bupropion Hydrochloride SR
- Generic name
- Bupropion hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079095
- Marketed since
- July 2, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0135-1 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-1) | Sep 11, 2019 |
| 71335-0135-2 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-2) | Sep 18, 2019 |
| 71335-0135-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-3) | Sep 11, 2019 |
| 71335-0135-4 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-4) | Oct 8, 2024 |
| 71335-0135-5 | 45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-5) | Oct 8, 2024 |
| 71335-0135-6 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-6) | Oct 8, 2024 |
| 71335-0135-7 | 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-7) | Oct 8, 2024 |
| 71335-0135-8 | 56 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-8) | Oct 8, 2024 |
| 71335-0135-9 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-9) | Oct 8, 2024 |
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