"37808-227-78" National Drug Code (NDC)

Rx Act Pain Relief 1 BOTTLE in 1 CARTON (37808-227-78) > 100 TABLET, COATED in 1 BOTTLE
(H E B)

NDC Code37808-227-78
Package Description1 BOTTLE in 1 CARTON (37808-227-78) > 100 TABLET, COATED in 1 BOTTLE
Product NDC37808-227
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act Pain Relief
Proprietary Name SuffixExtra Strength
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20060106
Marketing Category NameOTC MONOGRAPH NOT FINAL
Application Numberpart343
ManufacturerH E B
Substance NameACETAMINOPHEN
Strength500
Strength Unitmg/1

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