Doxazosin - 68788-9675-3 - (Doxazosin)

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Drug Information of Doxazosin

Product NDC: 68788-9675
Proprietary Name: Doxazosin
Non Proprietary Name: Doxazosin
Active Ingredient(s): 2    mg/1 & nbsp;   Doxazosin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Doxazosin

Product NDC: 68788-9675
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075580
Marketing Category: ANDA
Start Marketing Date: 20130624

Package Information of Doxazosin

Package NDC: 68788-9675-3
Package Description: 30 TABLET in 1 BOTTLE (68788-9675-3)

NDC Information of Doxazosin

NDC Code 68788-9675-3
Proprietary Name Doxazosin
Package Description 30 TABLET in 1 BOTTLE (68788-9675-3)
Product NDC 68788-9675
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxazosin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130624
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name DOXAZOSIN MESYLATE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Doxazosin


General Information