"61786-829-05" National Drug Code (NDC)

Metronidazole 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61786-829-05)
(REMEDYREPACK INC.)

NDC Code61786-829-05
Package Description21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61786-829-05)
Product NDC61786-829
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetronidazole
Non-Proprietary NameMetronidazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160825
Marketing Category NameANDA
Application NumberANDA203458
ManufacturerREMEDYREPACK INC.
Substance NameMETRONIDAZOLE
Strength250
Strength Unitmg/1
Pharmacy ClassesNitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient]

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