Bupropion Hydrochloride Sr 43547-0290
Generic: Bupropion Hydrochloride
Product NDC
43547-0290- Manufacturer
- Solco Healthcare Us Llc
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 1, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA202304
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 200 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(4)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-06)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-09)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-10)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-50)