"70518-0163-2" National Drug Code (NDC)

Famotidine 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0163-2)
(REMEDYREPACK INC.)

NDC Code70518-0163-2
Package Description60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0163-2)
Product NDC70518-0163
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170120
Marketing Category NameANDA
Application NumberANDA075511
ManufacturerREMEDYREPACK INC.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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