Bupropion Hydrochloride 69292-0602
Product NDC
69292-0602- Manufacturer
- Amici Pharma, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 21, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA075584
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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(1)
100 TABLET, FILM COATED in 1 BOTTLE (69292-602-01)