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"52125-780-05" National Drug Code (NDC)

Ibuprofen 21 TABLET in 1 BLISTER PACK (52125-780-05)
(REMEDYREPACK INC.)

NDC Code52125-780-05
Package Description21 TABLET in 1 BLISTER PACK (52125-780-05)
Product NDC52125-780
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20131115
End Marketing Date20170922
Marketing Category NameANDA
Application NumberANDA090796
ManufacturerREMEDYREPACK INC.
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-780-05





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