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"37808-517-71" National Drug Code (NDC)

Rx Act Ibuprofen 1 BOTTLE in 1 CARTON (37808-517-71) > 50 TABLET, FILM COATED in 1 BOTTLE
(H E B)

NDC Code37808-517-71
Package Description1 BOTTLE in 1 CARTON (37808-517-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC37808-517
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act Ibuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20060704
Marketing Category NameANDA
Application NumberANDA077349
ManufacturerH E B
Substance NameIBUPROFEN
Strength200
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-517-71





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