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Doxazosin Mesylate - 53808-0361-1 - (Doxazosin Mesylate)

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Drug Information of Doxazosin Mesylate

Product NDC: 53808-0361
Proprietary Name: Doxazosin Mesylate
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 Mesylate

Product NDC: 53808-0361
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075536
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Doxazosin Mesylate

Package NDC: 53808-0361-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0361-1)

NDC Information of Doxazosin Mesylate

NDC Code 53808-0361-1
Proprietary Name Doxazosin Mesylate
Package Description 30 TABLET in 1 BLISTER PACK (53808-0361-1)
Product NDC 53808-0361
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxazosin Mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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 Mesylate


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