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"37808-217-71" National Drug Code (NDC)

Rx Act Pain Relief 8 Hr 1 BOTTLE in 1 CARTON (37808-217-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
(H E B)

NDC Code37808-217-71
Package Description1 BOTTLE in 1 CARTON (37808-217-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC37808-217
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act Pain Relief 8 Hr
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20051001
Marketing Category NameANDA
Application NumberANDA075077
ManufacturerH E B
Substance NameACETAMINOPHEN
Strength650
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-217-71





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