"70882-130-21" National Drug Code (NDC)

Metronidazole250 Mg 21 TABLET, FILM COATED in 1 BOTTLE (70882-130-21)
(Cambridge Therapeutics Technologies, LLC)

NDC Code70882-130-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE (70882-130-21)
Product NDC70882-130
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetronidazole250 Mg
Proprietary Name Suffix250 Mg
Non-Proprietary NameMetronidazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160613
Marketing Category NameANDA
Application NumberANDA070040
ManufacturerCambridge Therapeutics Technologies, LLC
Substance NameMETRONIDAZOLE
Strength250
Strength Unitmg/1
Pharmacy ClassesNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]

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