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"63629-8891-2" National Drug Code (NDC)

Ibuprofen And Famotidine 90 TABLET, FILM COATED in 1 BOTTLE (63629-8891-2)
(Bryant Ranch Prepack)

NDC Code63629-8891-2
Package Description90 TABLET, FILM COATED in 1 BOTTLE (63629-8891-2)
Product NDC63629-8891
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
ManufacturerBryant Ranch Prepack
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/63629-8891-2





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