Bupropion Hydrochloride 71610-0774
Product NDC
71610-0774- Manufacturer
- Aphena Pharma Solutions - Tennessee, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 17, 2006
- Listing Expires
- December 31, 2026
- Application
- ANDA076143
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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(4)
60 TABLET, FILM COATED in 1 BOTTLE (71610-774-53)
120 TABLET, FILM COATED in 1 BOTTLE (71610-774-70)
180 TABLET, FILM COATED in 1 BOTTLE (71610-774-80)
360 TABLET, FILM COATED in 1 BOTTLE (71610-774-94)