NDC 71335-1870 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 200 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-1870
Product details
- Brand name
- Bupropion Hydrochloride SR
- Generic name
- Bupropion hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211347
- Marketed since
- November 2, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1870-1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-1) | May 24, 2021 |
| 71335-1870-2 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-2) | Jul 18, 2024 |
| 71335-1870-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-3) | Jul 18, 2024 |
| 71335-1870-4 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-4) | Jul 18, 2024 |
| 71335-1870-5 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-5) | Jul 18, 2024 |
| 71335-1870-6 | 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-6) | Jul 18, 2024 |
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