"61919-363-30" National Drug Code (NDC)

Metronidazole 30 TABLET, FILM COATED in 1 BOTTLE (61919-363-30)
(DIRECT RX)

NDC Code61919-363-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (61919-363-30)
Product NDC61919-363
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetronidazole
Non-Proprietary NameMetronidazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180314
Marketing Category NameANDA
Application NumberANDA070044
ManufacturerDIRECT RX
Substance NameMETRONIDAZOLE
Strength500
Strength Unitmg/1
Pharmacy ClassesNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]

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