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"72657-112-20" National Drug Code (NDC)

Famotidine 1 BOTTLE in 1 CARTON (72657-112-20) / 200 TABLET, FILM COATED in 1 BOTTLE
(GLENMARK THERAPEUTICS INC., USA)

NDC Code72657-112-20
Package Description1 BOTTLE in 1 CARTON (72657-112-20) / 200 TABLET, FILM COATED in 1 BOTTLE
Product NDC72657-112
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220601
Marketing Category NameANDA
Application NumberANDA215822
ManufacturerGLENMARK THERAPEUTICS INC., USA
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72657-112-20





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