Bupropion Hydrochloride Sr 70436-0059
Generic: Bupropion Hydrochloride
Product NDC
70436-0059- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 2, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA211347
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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(4)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-01)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-02)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-05)
250 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-22)