Bupropion Hydrochloride 70010-0785
Product NDC
70010-0785- Manufacturer
- Granules Pharmaceuticals Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 15, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA215568
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 300 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(3)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-03)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-05)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-09)