"61919-032-14" National Drug Code (NDC)

Metronidazole 14 TABLET, FILM COATED in 1 BOTTLE (61919-032-14)
(DIRECT RX)

NDC Code61919-032-14
Package Description14 TABLET, FILM COATED in 1 BOTTLE (61919-032-14)
Product NDC61919-032
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetronidazole
Non-Proprietary NameMetronidazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170214
Marketing Category NameANDA
Application NumberANDA203458
ManufacturerDIRECT RX
Substance NameMETRONIDAZOLE
Strength500
Strength Unitmg/1
Pharmacy ClassesNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]

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