"53002-3010-3" National Drug Code (NDC)

Ibu 20 TABLET in 1 BOTTLE (53002-3010-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-3010-3
Package Description20 TABLET in 1 BOTTLE (53002-3010-3)
Product NDC53002-3010
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbu
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20081120
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerRPK Pharmaceuticals, 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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