Alfuzosin Hydrochloride 47335-0956
Product NDC
47335-0956- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 22, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA079057
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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(5)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-81)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-83)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88)