"51655-553-52" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-553-52)
(Northwind Pharmaceuticals)

NDC Code51655-553-52
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-553-52)
Product NDC51655-553
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210120
Marketing Category NameANDA
Application NumberANDA206530
ManufacturerNorthwind Pharmaceuticals
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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