NDCFind

Alfuzosin Hydrochloride 71335-2578-03

Package NDC

71335-2578-03

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
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Active Ingredients

IngredientStrength
Alfuzosin Hydrochloride10 mg/1

Drug Class

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

Selected Package

71335-2578-03Selected

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-3)

Other packages for this product(4)

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-1)

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-2)

120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-4)

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2578-5)