"71205-535-10" National Drug Code (NDC)

Famotidine 10 TABLET, FILM COATED in 1 BOTTLE (71205-535-10)
(Proficient Rx LP)

NDC Code71205-535-10
Package Description10 TABLET, FILM COATED in 1 BOTTLE (71205-535-10)
Product NDC71205-535
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20151222
Marketing Category NameANDA
Application NumberANDA206530
ManufacturerProficient Rx LP
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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