"68001-398-03" National Drug Code (NDC)

Famotidine 500 TABLET, FILM COATED in 1 BOTTLE (68001-398-03)
(BluePoint Laboratories)

NDC Code68001-398-03
Package Description500 TABLET, FILM COATED in 1 BOTTLE (68001-398-03)
Product NDC68001-398
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190619
Marketing Category NameANDA
Application NumberANDA206530
ManufacturerBluePoint Laboratories
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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