NDC 71335-1044 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-1044
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210497
- Marketed since
- November 8, 2018
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1044-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-1) | Jan 3, 2019 |
| 71335-1044-2 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-2) | Jun 10, 2020 |
| 71335-1044-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-3) | Feb 28, 2019 |
| 71335-1044-4 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-4) | Dec 28, 2021 |
| 71335-1044-5 | 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1044-5) | Dec 28, 2021 |
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