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"67877-738-33" National Drug Code (NDC)

Ibuprofen 1 BLISTER PACK in 1 CARTON (67877-738-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Ascend Laboratories, LLC)

NDC Code67877-738-33
Package Description1 BLISTER PACK in 1 CARTON (67877-738-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC67877-738
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260915
Marketing Category NameANDA
Application NumberANDA214699
ManufacturerAscend Laboratories, LLC
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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