Nitroglycerin
Nitroglycerin Transdermal System
Approved
Approval ID
a1648bd9-8a89-4292-b703-aa83d9bd6c6d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 1, 2011
Manufacturers
FDA
Kremers Urban Pharmaceuticals Inc.
DUNS: 006422406
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Nitroglycerin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code62175-123
Application NumberANDA075115
Product Classification
M
Marketing Category
C73584
G
Generic Name
Nitroglycerin
Product Specifications
Route of AdministrationTRANSDERMAL
Effective DateOctober 25, 2007
FDA Product Classification
INGREDIENTS (1)
NitroglycerinActive
Quantity: 20.8 mg in 1 1
Code: G59M7S0WS3
Classification: ACTIB
Nitroglycerin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code62175-124
Application NumberANDA075115
Product Classification
M
Marketing Category
C73584
G
Generic Name
Nitroglycerin
Product Specifications
Route of AdministrationTRANSDERMAL
Effective DateOctober 25, 2007
FDA Product Classification
INGREDIENTS (1)
NitroglycerinActive
Quantity: 37.4 mg in 1 1
Code: G59M7S0WS3
Classification: ACTIB