Ibuprofen
Ibuprofen 800 MG
Approved
Approval ID
dcd6507e-c15b-4035-ac3d-4d414fcf958a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 1, 2015
Manufacturers
FDA
Northwind Pharmaceuticals
DUNS: 036986393
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ibuprofen
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51655-051
Application NumberANDA078558
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ibuprofen
Product Specifications
Route of AdministrationORAL
Effective DateApril 1, 2015
FDA Product Classification
INGREDIENTS (1)
IBUPROFENActive
Quantity: 800 mg in 1 1
Code: WK2XYI10QM
Classification: ACTIB