Bupropion Hydrochloride Sr 51655-0115
Generic: Bupropion Hydrochloride
Product NDC
51655-0115- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 5, 2022
- Listing Expires
- December 31, 2027
- 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)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-25)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-26)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-52)
180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-83)