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"67877-626-90" National Drug Code (NDC)

Ibuprofen And Famotidine 90 TABLET, FILM COATED in 1 BOTTLE (67877-626-90)
(Ascend Laboratories, LLC)

NDC Code67877-626-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (67877-626-90)
Product NDC67877-626
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen And Famotidine
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210804
Marketing Category NameANDA
Application NumberANDA211890
ManufacturerAscend Laboratories, LLC
Substance NameFAMOTIDINE; IBUPROFEN
Strength26.6; 800
Strength Unitmg/1; mg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]

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