FDA.reportPublic FDA data

Application 090837

Type
ANDA
Sponsor
WOCKHARDT

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001FAMOTIDINEFAMOTIDINETABLET;ORAL20MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
55648-374FAMOTIDINEFAMOTIDINEWOCKHARDT LIMITEDANDACurrent
64679-374FAMOTIDINEfamotidineWockhardt USA LLC.ANDACurrent
64679-374FAMOTIDINEfamotidineWockhardt USA LLC.ANDACurrent