"37808-709-71" National Drug Code (NDC)

Ibuprofen 1 BOTTLE in 1 CARTON (37808-709-71) / 50 TABLET, FILM COATED in 1 BOTTLE
(H E B)

NDC Code37808-709-71
Package Description1 BOTTLE in 1 CARTON (37808-709-71) / 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC37808-709
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen
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
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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