Bupropion Hydrochloride 72789-0301
Product NDC
72789-0301- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 8, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA210497
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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(1)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-301-90)