"49884-366-09" National Drug Code (NDC)

Ibuprofen And Famotidine 90 TABLET in 1 BOTTLE (49884-366-09)
(ENDO USA, Inc.)

NDC Code49884-366-09
Package Description90 TABLET in 1 BOTTLE (49884-366-09)
Product NDC49884-366
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen And Famotidine
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20240322
Marketing Category NameANDA
Application NumberANDA203658
ManufacturerENDO USA, Inc.
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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