Bupropion Hydrochloride 47335-0954
Product NDC
47335-0954- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 25, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA200695
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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, EXTENDED RELEASE in 1 BOTTLE (47335-954-13)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-81)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-83)