Bupropion Hydrochloride 00904-6636
Product NDC
00904-6636- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 17, 2006
- Listing Expires
- December 31, 2027
- Application
- ANDA076143
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 100 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(1)
100 BLISTER PACK in 1 CARTON (0904-6636-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK