Clemastine Fumarate
Clemastine Fumarate
Approved
Approval ID
be4f8613-e4da-45e1-a5c0-e9337ca5d245
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 21, 2014
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.
Clemastine Fumarate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51655-425
Application NumberANDA073283
Product Classification
M
Marketing Category
C73584
G
Generic Name
Clemastine Fumarate
Product Specifications
Route of AdministrationOral
Effective DateJuly 21, 2014
FDA Product Classification
INGREDIENTS (1)
CLEMASTINE FUMARATEActive
Quantity: 2.68 mg in 1 1
Code: 19259EGQ3D
Classification: ACTIB