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"71335-1218-0" National Drug Code (NDC)

Ibuprofen 21 TABLET, FILM COATED in 1 BOTTLE (71335-1218-0)
(Bryant Ranch Prepack)

NDC Code71335-1218-0
Package Description21 TABLET, FILM COATED in 1 BOTTLE (71335-1218-0)
Product NDC71335-1218
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20151221
Marketing Category NameANDA
Application NumberANDA091625
ManufacturerBryant Ranch Prepack
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1218-0





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