Bupropion Hydrochloride 62135-0723
Product NDC
62135-0723- Manufacturer
- Chartwell Rx, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 19, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA206975
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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)
90 TABLET in 1 BOTTLE (62135-723-90)