NDC 71335-1702 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71335-1702
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 · ANDA205794
- Marketed since
- April 20, 2018
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 71335-1702-1 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-1) | Sep 16, 2020 |
| 71335-1702-2 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-2) | Nov 20, 2020 |
| 71335-1702-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-3) | Oct 6, 2020 |
| 71335-1702-4 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-4) | Apr 4, 2024 |
| 71335-1702-5 | 45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-5) | Apr 4, 2024 |
| 71335-1702-6 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-6) | Sep 8, 2020 |
| 71335-1702-7 | 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-7) | Apr 4, 2024 |
| 71335-1702-8 | 56 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-8) | Apr 4, 2024 |
| 71335-1702-9 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-9) | Apr 4, 2024 |
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