Bupropion Hydrochloride Xl 69367-0288
Generic: Bupropion Hydrochloride
Product NDC
69367-0288- Manufacturer
- Westminster Pharmaceuticals, Llc
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA207224
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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(2)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-288-05)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-288-09)