Doxazosin mesylate
DOXAZOSIN MESYLATE TABLETS, USP
Approved
Approval ID
98a248f5-a79b-43ba-839f-014a77edf9c2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 3, 2015
Manufacturers
FDA
State of Florida DOH Central Pharmacy
DUNS: 829348114
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
doxazosin mesylate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code53808-1017
Application NumberANDA076161
Product Classification
M
Marketing Category
C73584
G
Generic Name
doxazosin mesylate
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 3, 2015
FDA Product Classification
INGREDIENTS (8)
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
DOXAZOSIN MESYLATEActive
Quantity: 2 mg in 1 1
Code: 86P6PQK0MU
Classification: ACTIM
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
LACTOSEInactive
Code: J2B2A4N98G
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8
Classification: IACT