Bupropion Hydrochloride 71335-0182
Product NDC
71335-0182- Manufacturer
- Bryant Ranch Prepack
- 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 | 100 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(7)
60 TABLET, FILM COATED in 1 BOTTLE (71335-0182-1)
30 TABLET, FILM COATED in 1 BOTTLE (71335-0182-2)
100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3)
90 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4)
120 TABLET, FILM COATED in 1 BOTTLE (71335-0182-5)
15 TABLET, FILM COATED in 1 BOTTLE (71335-0182-6)
21 TABLET, FILM COATED in 1 BOTTLE (71335-0182-7)