"37000-517-08" National Drug Code (NDC)

Vicks Dayquil Severe 1 BLISTER PACK in 1 CARTON (37000-517-08) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
(The Procter & Gamble Manufacturing Company)

NDC Code37000-517-08
Package Description1 BLISTER PACK in 1 CARTON (37000-517-08) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC37000-517
Product Type NameHUMAN OTC DRUG
Proprietary NameVicks Dayquil Severe
Proprietary Name SuffixCold And Flu
Non-Proprietary NameAcetaminophen, Phenylephine Hcl, Dextromethorphan Hydrobromide, And Guaifenesin
Dosage FormCAPSULE, LIQUID FILLED
UsageORAL
Start Marketing Date20180710
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM012
ManufacturerThe Procter & Gamble Manufacturing Company
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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