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Doxazosin Mesylate - 67253-382-09 - (Doxazosin Mesylate)

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Drug Information of Doxazosin Mesylate

Product NDC: 67253-382
Proprietary Name: Doxazosin Mesylate
Non Proprietary Name: Doxazosin Mesylate
Active Ingredient(s): 4    mg/1 & nbsp;   Doxazosin Mesylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Doxazosin Mesylate

Product NDC: 67253-382
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076161
Marketing Category: ANDA
Start Marketing Date: 20040610

Package Information of Doxazosin Mesylate

Package NDC: 67253-382-09
Package Description: 90 TABLET in 1 BOTTLE (67253-382-09)

NDC Information of Doxazosin Mesylate

NDC Code 67253-382-09
Proprietary Name Doxazosin Mesylate
Package Description 90 TABLET in 1 BOTTLE (67253-382-09)
Product NDC 67253-382
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxazosin Mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040610
Marketing Category Name ANDA
Labeler Name DAVA Pharmaceuticals, Inc.
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 Mesylate


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