Bupropion Hydrochloride 72241-0020
Product NDC
72241-0020- Manufacturer
- Modavar Pharmaceuticals Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 16, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA208606
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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(3)
100 TABLET, FILM COATED in 1 BOTTLE (72241-020-05)
1000 TABLET, FILM COATED in 1 BOTTLE (72241-020-11)
10 BLISTER PACK in 1 CARTON (72241-020-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK