"52125-698-03" National Drug Code (NDC)

Ibuprofen 20 TABLET in 1 BLISTER PACK (52125-698-03)
(REMEDYREPACK INC.)

NDC Code52125-698-03
Package Description20 TABLET in 1 BLISTER PACK (52125-698-03)
Product NDC52125-698
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20131101
Marketing Category NameANDA
Application NumberANDA090796
ManufacturerREMEDYREPACK INC.
Substance NameIBUPROFEN
Strength400
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

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