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"71335-0746-9" National Drug Code (NDC)

Sunmark Ibuprofen 56 TABLET, FILM COATED in 1 BOTTLE (71335-0746-9)
(Bryant Ranch Prepack)

NDC Code71335-0746-9
Package Description56 TABLET, FILM COATED in 1 BOTTLE (71335-0746-9)
Product NDC71335-0746
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Ibuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20030624
Marketing Category NameANDA
Application NumberANDA072096
ManufacturerBryant Ranch Prepack
Substance NameIBUPROFEN
Strength200
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/71335-0746-9





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