Bupropion Hydrochloride 72789-0070
Product NDC
72789-0070- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- 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(2)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90)