"70000-0289-1" National Drug Code (NDC)

Severe Cold And Flu 1 BLISTER PACK in 1 CARTON (70000-0289-1) / 12 TABLET, FILM COATED in 1 BLISTER PACK
(Cardinal Health 110, LLC. DBA Leader)

NDC Code70000-0289-1
Package Description1 BLISTER PACK in 1 CARTON (70000-0289-1) / 12 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC70000-0289
Product Type NameHUMAN OTC DRUG
Proprietary NameSevere Cold And Flu
Proprietary Name SuffixMaximum Strength, Daytime, Non-drowsy
Non-Proprietary NameAcetaminophen. Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140227
End Marketing Date20250131
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM012
ManufacturerCardinal Health 110, LLC. DBA Leader
Substance NameACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 200; 5
Strength Unitmg/1; mg/1; mg/1; mg/1
Pharmacy ClassesAdrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]

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