"70934-819-60" National Drug Code (NDC)

Famotidine 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-819-60)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-819-60
Package Description60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-819-60)
Product NDC70934-819
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210126
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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