Alfuzosin Hydrochloride

Product NDC

42291-110

11-digit product format

422910110

Labeler code

42291

Product ID

42291-110_7b0b07af-2e83-da84-e053-2991aa0a8c13

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Alfuzosin Hydrochloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA079013

Marketing category

ANDA

Marketing start

2012-03-13

Marketing end

2019-04-30

Substance

ALFUZOSIN HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record