Bupropion Hydrochloride 68001-0613
Product NDC
68001-0613- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 8, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA215568
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 150 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(3)
500 TABLET in 1 BOTTLE (68001-613-03)
30 TABLET in 1 BOTTLE (68001-613-04)
90 TABLET in 1 BOTTLE (68001-613-05)