TERAZOSIN
TERAZOSIN
Approved
Approval ID
3109caa1-3388-41b4-ab9a-aee009c7326d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 19, 2015
Manufacturers
FDA
Northwind Pharmaceuticals, LLC
DUNS: 036986393
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
terazosin hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51655-676
Application NumberANDA075317
Product Classification
M
Marketing Category
C73584
G
Generic Name
terazosin hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateMarch 19, 2015
FDA Product Classification
INGREDIENTS (1)
TERAZOSIN HYDROCHLORIDEActive
Quantity: 5 mg in 1 1
Code: D32S14F082
Classification: ACTIM