"71335-0617-2" National Drug Code (NDC)

Oxaprozin 20 TABLET in 1 BOTTLE (71335-0617-2)
(Bryant Ranch Prepack)

NDC Code71335-0617-2
Package Description20 TABLET in 1 BOTTLE (71335-0617-2)
Product NDC71335-0617
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxaprozin
Non-Proprietary NameOxaprozin
Dosage FormTABLET
UsageORAL
Start Marketing Date20170504
Marketing Category NameANDA
Application NumberANDA208633
ManufacturerBryant Ranch Prepack
Substance NameOXAPROZIN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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