Bupropion Hydrochloride Xl 70436-0011
Generic: Bupropion Hydrochloride
Product NDC
70436-0011- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 1, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210015
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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)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-011-02)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-011-04)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-011-06)