"52125-673-04" National Drug Code (NDC)

Ibuprofen 14 TABLET in 1 BLISTER PACK (52125-673-04)
(REMEDYREPACK INC.)

NDC Code52125-673-04
Package Description14 TABLET in 1 BLISTER PACK (52125-673-04)
Product NDC52125-673
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20130717
End Marketing Date20171003
Marketing Category NameANDA
Application NumberANDA090796
ManufacturerREMEDYREPACK 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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