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"37808-227-71" National Drug Code (NDC)

Rx Act Pain Relief 1 BOTTLE in 1 CARTON (37808-227-71) > 50 TABLET, COATED in 1 BOTTLE
(H E B)

NDC Code37808-227-71
Package Description1 BOTTLE in 1 CARTON (37808-227-71) > 50 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

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-227-71





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