"0536-1089-01" National Drug Code (NDC)

Ibuprofen 1 BOTTLE in 1 CARTON (0536-1089-01) > 100 TABLET, FILM COATED in 1 BOTTLE
(Rugby Laboratories)

NDC Code0536-1089-01
Package Description1 BOTTLE in 1 CARTON (0536-1089-01) > 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC0536-1089
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19880524
End Marketing Date20221106
Marketing Category NameANDA
Application NumberANDA075010
ManufacturerRugby Laboratories
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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