Cardura - 0049-2750-41 - (doxazosin mesylate)

Alphabetical Index


Drug Information of Cardura

Product NDC: 0049-2750
Proprietary Name: Cardura
Non Proprietary Name: doxazosin mesylate
Active Ingredient(s): 1    mg/1 & nbsp;   doxazosin mesylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Cardura

Product NDC: 0049-2750
Labeler Name: Roerig
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019668
Marketing Category: NDA
Start Marketing Date: 19901102

Package Information of Cardura

Package NDC: 0049-2750-41
Package Description: 100 TABLET in 1 PACKAGE (0049-2750-41)

NDC Information of Cardura

NDC Code 0049-2750-41
Proprietary Name Cardura
Package Description 100 TABLET in 1 PACKAGE (0049-2750-41)
Product NDC 0049-2750
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxazosin mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19901102
Marketing Category Name NDA
Labeler Name Roerig
Substance Name DOXAZOSIN MESYLATE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Cardura


General Information