"58602-706-62" National Drug Code (NDC)

Famotidine 5 BLISTER PACK in 1 CARTON (58602-706-62) > 5 TABLET, FILM COATED in 1 BLISTER PACK (58602-706-60)
(Aurohealth LLC)

NDC Code58602-706-62
Package Description5 BLISTER PACK in 1 CARTON (58602-706-62) > 5 TABLET, FILM COATED in 1 BLISTER PACK (58602-706-60)
Product NDC58602-706
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160426
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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