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"85509-1315-9" National Drug Code (NDC)

Ibuprofen And Famotidine 90 TABLET in 1 BOTTLE (85509-1315-9)
(PHOENIX RX LLC)

NDC Code85509-1315-9
Package Description90 TABLET in 1 BOTTLE (85509-1315-9)
Product NDC85509-1315
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen And Famotidine
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20230315
Marketing Category NameANDA
Application NumberANDA216814
ManufacturerPHOENIX RX 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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/85509-1315-9





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