Bupropion Hydrochloride 51655-0390
Product NDC
51655-0390- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 28, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA206975
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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)
60 TABLET in 1 BOTTLE, PLASTIC (51655-390-25)
90 TABLET in 1 BOTTLE, PLASTIC (51655-390-26)