Bupropion Hydrochloride 71209-0053-17
- Manufacturer
- Cadila Pharmaceuticals Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 16, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA208606
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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]
Selected Package
71209-0053-17Selected10 BLISTER PACK in 1 CARTON (71209-053-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Other packages for this product(2)
100 TABLET, FILM COATED in 1 BOTTLE (71209-053-05)
1000 TABLET, FILM COATED in 1 BOTTLE (71209-053-11)