Bupropion Hydrochloride 70010-0125
Product NDC
70010-0125- 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
Need to source Bupropion Hydrochloride? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 100 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(3)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-125-03)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-125-05)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-125-06)