Bupropion Hydrochloride 60687-0340
Product NDC
60687-0340- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 1, 2018
- 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(1)
100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-340-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-340-11)