Doxazosin - 60505-0095-1 - (Doxazosin)

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Drug Information of Doxazosin

Product NDC: 60505-0095
Proprietary Name: Doxazosin
Non Proprietary Name: Doxazosin
Active Ingredient(s): 4    mg/1 & nbsp;   Doxazosin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Doxazosin

Product NDC: 60505-0095
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075580
Marketing Category: ANDA
Start Marketing Date: 20110714

Package Information of Doxazosin

Package NDC: 60505-0095-1
Package Description: 1000 TABLET in 1 BOTTLE (60505-0095-1)

NDC Information of Doxazosin

NDC Code 60505-0095-1
Proprietary Name Doxazosin
Package Description 1000 TABLET in 1 BOTTLE (60505-0095-1)
Product NDC 60505-0095
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxazosin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110714
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name DOXAZOSIN MESYLATE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Doxazosin


General Information