NDC 51655-390 – bupropion Hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet · Oral
Product NDC51655-390
Product details
- Brand name
- bupropion Hydrochloride
- Generic name
- bupropion Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA206975
- Marketed since
- January 28, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51655-390-25 | 60 TABLET in 1 BOTTLE, PLASTIC (51655-390-25) | Jan 28, 2022 |
| 51655-390-26 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-390-26) | Jan 28, 2022 |
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