"58602-859-34" National Drug Code (NDC)

Famotidine 1 BOTTLE in 1 CARTON (58602-859-34) > 200 TABLET, FILM COATED in 1 BOTTLE
(Aurohealth LLC)

NDC Code58602-859-34
Package Description1 BOTTLE in 1 CARTON (58602-859-34) > 200 TABLET, FILM COATED in 1 BOTTLE
Product NDC58602-859
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210302
Marketing Category NameANDA
Application NumberANDA206531
ManufacturerAurohealth LLC
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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