"67296-0913-1" National Drug Code (NDC)

Ibu 30 TABLET in 1 BOTTLE (67296-0913-1)
(RedPharm Drug, Inc.)

NDC Code67296-0913-1
Package Description30 TABLET in 1 BOTTLE (67296-0913-1)
Product NDC67296-0913
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbu
Non-Proprietary NameIbu
Dosage FormTABLET
UsageORAL
Start Marketing Date20081120
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerRedPharm Drug, Inc.
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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