Bupropion Hydrochloride 00904-7529
Product NDC
00904-7529- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 30, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA206975
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 75 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(1)
100 TABLET in 1 BOTTLE (0904-7529-60)