"10768-7522-2" National Drug Code (NDC)

Ibuprofen 500 TABLET in 1 BOTTLE (10768-7522-2)
(Perrigo Pharmaceuticals Company)

NDC Code10768-7522-2
Package Description500 TABLET in 1 BOTTLE (10768-7522-2)
Product NDC10768-7522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20060508
Marketing Category NameANDA
Application NumberANDA077114
ManufacturerPerrigo Pharmaceuticals Company
Substance NameIBUPROFEN
Strength800
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

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