Application 075512

Type
ANDA
Sponsor
P AND L

Related Records

Application Products

ProductDrugIngredientFormStrengthReference drugReference standard
001FAMOTIDINEFAMOTIDINETABLET;ORAL10MGNoNo

NDC Listings For This Application

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