Alfuzosin Hydrochloride 72162-1449
Product NDC
72162-1449- Manufacturer
- Bryant Ranch Prepack
- 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(1)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1449-9)