Bupropion Hydrochloride 70010-0127-06
- Manufacturer
- Granules Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 31, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA218385
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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]
Selected Package
70010-0127-06Selected60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-127-06)
Other packages for this product(2)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-127-03)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-127-05)