Bupropion Hydrochloride (xl) 43598-0656
Generic: Bupropion Hydrochloride
Product NDC
43598-0656- Manufacturer
- Dr Reddys Laboratories Inc
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 12, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA207479
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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, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-05)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-30)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-90)