Bupropion Hydrochloride 50090-5245
Product NDC
50090-5245- Manufacturer
- A-S Medication Solutions
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 25, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA210497
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 300 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(2)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5245-0)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5245-1)