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"0025-1381-51" National Drug Code (NDC)

Daypro 500 TABLET, FILM COATED in 1 BOTTLE (0025-1381-51)
(Pfizer Laboratories Div Pfizer Inc)

NDC Code0025-1381-51
Package Description500 TABLET, FILM COATED in 1 BOTTLE (0025-1381-51)
Product NDC0025-1381
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDaypro
Non-Proprietary NameOxaprozin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19921029
Marketing Category NameNDA
Application NumberNDA018841
ManufacturerPfizer Laboratories Div Pfizer Inc
Substance NameOXAPROZIN
Strength600
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0025-1381-51





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