Application 071163

Type
ANDA
Sponsor
OHM

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001IBUPROFENIBUPROFENTABLET;ORAL200MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
63739-134IbuprofenIbuprofenMcKesson Packaging Services Business Unit of McKesson CorporationANDACurrent