"37808-437-71" National Drug Code (NDC)

Rx Act Pain Relief 1 BOTTLE in 1 CARTON (37808-437-71) > 50 TABLET, FILM COATED in 1 BOTTLE
(H E B)

NDC Code37808-437-71
Package Description1 BOTTLE in 1 CARTON (37808-437-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC37808-437
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act Pain Relief
Proprietary Name SuffixPm
Non-Proprietary NameAcetaminophen, Diphenhydramine Hcl
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19960710
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart338
ManufacturerH E B
Substance NameACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength500; 25
Strength Unitmg/1; mg/1

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