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"70518-0490-0" National Drug Code (NDC)

Ibu 30 TABLET in 1 BLISTER PACK (70518-0490-0)
(REMEDYREPACK INC.)

NDC Code70518-0490-0
Package Description30 TABLET in 1 BLISTER PACK (70518-0490-0)
Product NDC70518-0490
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbu
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20171115
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerREMEDYREPACK INC.
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0490-0





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