"61919-499-21" National Drug Code (NDC)

Metronidazole 21 TABLET, FILM COATED in 1 BOTTLE (61919-499-21)
(DIRECT RX)

NDC Code61919-499-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE (61919-499-21)
Product NDC61919-499
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetronidazole
Non-Proprietary NameMetronidazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180326
Marketing Category NameANDA
Application NumberANDA203458
ManufacturerDIRECT RX
Substance NameMETRONIDAZOLE
Strength250
Strength Unitmg/1
Pharmacy ClassesNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]

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