NDCFind

Alfuzosin Hydrochloride 71335-2146-02

Package NDC

71335-2146-02

Product NDC: 71335-2146

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

IngredientStrength
Alfuzosin Hydrochloride10 mg/1

Drug Class

Adrenergic alpha-Antagonists [MoA]alpha-Adrenergic Blocker [EPC]

Selected Package

71335-2146-02Selected

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-2)

Other packages for this product(4)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-1)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-3)

120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-4)

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2146-5)