"53002-2199-5" National Drug Code (NDC)

Famotidine 15 TABLET, FILM COATED in 1 BOTTLE (53002-2199-5)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-2199-5
Package Description15 TABLET, FILM COATED in 1 BOTTLE (53002-2199-5)
Product NDC53002-2199
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20151222
Marketing Category NameANDA
Application NumberANDA206530
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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