Alfuzosin Hydrochloride 71335-2578
Product NDC
71335-2578- Manufacturer
- Bryant Ranch Prepack
- 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
Need to source Alfuzosin Hydrochloride? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Alfuzosin Hydrochloride | 10 mg/1 |
Drug Class
Adrenergic alpha-Antagonists [MoA]alpha-Adrenergic Blocker [EPC]
Packaging Options(5)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-1)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-2)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-3)
120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-4)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-5)