"52959-077-21" National Drug Code (NDC)

Ibuprofen 21 TABLET in 1 BOTTLE (52959-077-21)
(H.J. Harkins Company, Inc.)

NDC Code52959-077-21
Package Description21 TABLET in 1 BOTTLE (52959-077-21)
Product NDC52959-077
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20091123
Marketing Category NameANDA
Application NumberANDA078558
ManufacturerH.J. Harkins Company, Inc.
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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