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Alfuzosin Hydrochloride - 65862-249-01 - (Alfuzosin Hydrochloride)

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Drug Information of Alfuzosin Hydrochloride

Product NDC: 65862-249
Proprietary Name: Alfuzosin Hydrochloride
Non Proprietary Name: Alfuzosin Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Alfuzosin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Alfuzosin Hydrochloride

Product NDC: 65862-249
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079060
Marketing Category: ANDA
Start Marketing Date: 20120830

Package Information of Alfuzosin Hydrochloride

Package NDC: 65862-249-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-01)

NDC Information of Alfuzosin Hydrochloride

NDC Code 65862-249-01
Proprietary Name Alfuzosin Hydrochloride
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-01)
Product NDC 65862-249
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alfuzosin Hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120830
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name ALFUZOSIN HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Alfuzosin Hydrochloride


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