Uroxatral - 54868-5046-0 - (alfuzosin hydrochloride)

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Drug Information of Uroxatral

Product NDC: 54868-5046
Proprietary Name: Uroxatral
Non Proprietary Name: alfuzosin hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   alfuzosin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Uroxatral

Product NDC: 54868-5046
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021287
Marketing Category: NDA
Start Marketing Date: 20040622

Package Information of Uroxatral

Package NDC: 54868-5046-0
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5046-0)

NDC Information of Uroxatral

NDC Code 54868-5046-0
Proprietary Name Uroxatral
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-5046-0)
Product NDC 54868-5046
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alfuzosin hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20040622
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALFUZOSIN HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Uroxatral


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