Application 075512

Type
ANDA
Sponsor
P AND L

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001FAMOTIDINEFAMOTIDINETABLET;ORAL10MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0093-2748FamotidineFamotidineTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-2748FamotidineFamotidineTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-2748FamotidineFamotidineTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-2748FamotidineFamotidineTeva Pharmaceuticals USA, Inc.ANDACurrent
63629-7909FamotidineFamotidineBryant Ranch PrepackANDACurrent