"55315-292-12" National Drug Code (NDC)

Ibuprofen 1 BOTTLE, PLASTIC in 1 CARTON (55315-292-12) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
(FRED'S, INC.)

NDC Code55315-292-12
Package Description1 BOTTLE, PLASTIC in 1 CARTON (55315-292-12) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC55315-292
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19880524
End Marketing Date20220408
Marketing Category NameANDA
Application NumberANDA075010
ManufacturerFRED'S, INC.
Substance NameIBUPROFEN
Strength200
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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