Bupropion Hydrochloride 72789-0544
Product NDC
72789-0544- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 19, 2016
- 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(1)
90 TABLET in 1 BOTTLE, PLASTIC (72789-544-90)