"71335-1922-4" National Drug Code (NDC)

Metronidazole 56 TABLET in 1 BOTTLE (71335-1922-4)
(Bryant Ranch Prepack)

NDC Code71335-1922-4
Package Description56 TABLET in 1 BOTTLE (71335-1922-4)
Product NDC71335-1922
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetronidazole
Non-Proprietary NameMetronidazole
Dosage FormTABLET
UsageORAL
Start Marketing Date20150529
Marketing Category NameANDA
Application NumberANDA203974
ManufacturerBryant Ranch Prepack
Substance NameMETRONIDAZOLE
Strength500
Strength Unitmg/1
Pharmacy ClassesNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]

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