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"70332-310-01" National Drug Code (NDC)

Oxaprozin 14 TABLET, FILM COATED in 1 BOTTLE (70332-310-01)
(California Pharmaceuticals LLC)

NDC Code70332-310-01
Package Description14 TABLET, FILM COATED in 1 BOTTLE (70332-310-01)
Product NDC70332-310
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxaprozin
Non-Proprietary NameOxaprozin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170701
Marketing Category NameANDA
Application NumberANDA075855
ManufacturerCalifornia Pharmaceuticals LLC
Substance NameOXAPROZIN
Strength600
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70332-310-01





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