"70518-1536-1" National Drug Code (NDC)

Metronidazole 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1536-1)
(REMEDYREPACK INC.)

NDC Code70518-1536-1
Package Description21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1536-1)
Product NDC70518-1536
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetronidazole
Non-Proprietary NameMetronidazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181015
Marketing Category NameANDA
Application NumberANDA203458
ManufacturerREMEDYREPACK INC.
Substance NameMETRONIDAZOLE
Strength250
Strength Unitmg/1
Pharmacy ClassesNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]

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