"49349-352-10" National Drug Code (NDC)

Ibuprofen 6 TABLET in 1 BLISTER PACK (49349-352-10)
(REMEDYREPACK INC.)

NDC Code49349-352-10
Package Description6 TABLET in 1 BLISTER PACK (49349-352-10)
Product NDC49349-352
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20130725
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerREMEDYREPACK INC.
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

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