Doxazosin - 50436-6311-1 - (Doxazosin Mesylate)

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Drug Information of Doxazosin

Product NDC: 50436-6311
Proprietary Name: Doxazosin
Non Proprietary Name: Doxazosin Mesylate
Active Ingredient(s): 8    mg/1 & nbsp;   Doxazosin Mesylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Doxazosin

Product NDC: 50436-6311
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075536
Marketing Category: ANDA
Start Marketing Date: 20001020

Package Information of Doxazosin

Package NDC: 50436-6311-1
Package Description: 30 TABLET in 1 BOTTLE (50436-6311-1)

NDC Information of Doxazosin

NDC Code 50436-6311-1
Proprietary Name Doxazosin
Package Description 30 TABLET in 1 BOTTLE (50436-6311-1)
Product NDC 50436-6311
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxazosin Mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20001020
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name DOXAZOSIN MESYLATE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Doxazosin


General Information