Bupropion Hydrochloride 59651-0848
Product NDC
59651-0848- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 3, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA090325
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 200 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(2)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-848-01)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-848-60)