Alfuzosin Hydrochloride 57237-0114
Product NDC
57237-0114- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 30, 2012
- Listing Expires
- December 31, 2027
- Application
- ANDA079060
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Alfuzosin Hydrochloride | 10 mg/1 |
Drug Class
Adrenergic alpha-Antagonists [MoA]alpha-Adrenergic Blocker [EPC]
Packaging Options(3)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-01)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-05)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (57237-114-90)