FDA.reportPublic FDA data

Application 072025

Type
ANDA
Sponsor
PAR PHARM

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001METAPROTERENOL SULFATEMETAPROTERENOL SULFATETABLET;ORAL20MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
49884-259Metaproterenol SulfateMetaproterenol SulfatePar Pharmaceutical, Inc.ANDACurrent
49884-259Metaproterenol SulfateMetaproterenol SulfatePar Pharmaceutical, Inc.ANDACurrent