Bupropion Hydrochloride 00115-6811
Product NDC
00115-6811- Manufacturer
- Amneal Pharmaceuticals Of New York Llc
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 1, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA077415
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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]
Packaging Options(3)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-02)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-08)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-10)