"49349-370-08" National Drug Code (NDC)

Ibuprofen 10 TABLET in 1 BLISTER PACK (49349-370-08)
(REMEDYREPACK INC.)

NDC Code49349-370-08
Package Description10 TABLET in 1 BLISTER PACK (49349-370-08)
Product NDC49349-370
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20110712
Marketing Category NameANDA
Application NumberANDA076112
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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