Bupropion Hydrochloride 47335-0738
Product NDC
47335-0738- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 1, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA078866
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 200 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(4)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-08)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-13)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-86)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-88)