NDC 23155-191 – bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet · Oral
Product NDC23155-191
Product details
- Brand name
- bupropion Hydrochloride
- Generic name
- bupropion Hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA206975
- Marketed since
- August 19, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 75 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 23155-191-01 | 100 TABLET in 1 BOTTLE (23155-191-01) | Aug 19, 2016 |
| 23155-191-10 | 1000 TABLET in 1 BOTTLE (23155-191-10) | Aug 19, 2016 |
Recalls mentioning this NDC
- D-0489-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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