"37808-660-26" National Drug Code (NDC)

Rx Act Ibuprofen 1 BOTTLE in 1 CARTON (37808-660-26) > 120 mL in 1 BOTTLE
(H E B)

NDC Code37808-660-26
Package Description1 BOTTLE in 1 CARTON (37808-660-26) > 120 mL in 1 BOTTLE
Product NDC37808-660
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act Ibuprofen
Non-Proprietary NameIbuprofen
Dosage FormSUSPENSION
UsageORAL
Start Marketing Date20020619
Marketing Category NameANDA
Application NumberANDA074937
ManufacturerH E B
Substance NameIBUPROFEN
Strength100
Strength Unitmg/5mL

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