NDC 50090-7511 – Bupropion Hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-7511
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075491
- Marketed since
- April 25, 2024
- 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 |
|---|---|---|
| 50090-7511-0 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-7511-0) | Feb 20, 2025 |
| 50090-7511-3 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7511-3) | Feb 20, 2025 |
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