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"72578-214-16" National Drug Code (NDC)

Ibuprofen And Famotidine 90 TABLET in 1 BOTTLE (72578-214-16)
(Viona Pharmaceuticals Inc)

NDC Code72578-214-16
Package Description90 TABLET in 1 BOTTLE (72578-214-16)
Product NDC72578-214
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen And Famotidine
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20250601
Marketing Category NameANDA
Application NumberANDA218684
ManufacturerViona Pharmaceuticals 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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72578-214-16





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