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"61919-032-21" National Drug Code (NDC)

Metronidazole 21 TABLET, FILM COATED in 1 BOTTLE (61919-032-21)
(Direct_Rx)

NDC Code61919-032-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE (61919-032-21)
Product NDC61919-032
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetronidazole
Non-Proprietary NameMetronidazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190821
Marketing Category NameANDA
Application NumberANDA203458
ManufacturerDirect_Rx
Substance NameMETRONIDAZOLE
Strength500
Strength Unitmg/1
Pharmacy ClassesNitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-032-21





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