"61786-798-05" National Drug Code (NDC)

Ibuprofen 21 TABLET, FILM COATED in 1 BLISTER PACK (61786-798-05)
(REMEDYREPACK INC.)

NDC Code61786-798-05
Package Description21 TABLET, FILM COATED in 1 BLISTER PACK (61786-798-05)
Product NDC61786-798
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160928
Marketing Category NameANDA
Application NumberANDA091625
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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