Bupropion Hydrochloride 63304-0723-90
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 9, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA200216
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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]
Selected Package
63304-0723-90Selected90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-723-90)
Other packages for this product(2)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-723-05)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-723-30)