Package 0025-1381-31

Brand: daypro

Generic: oxaprozin
NDC Package

Package Facts

Identity

Package NDC 0025-1381-31
Digits Only 0025138131
Product NDC 0025-1381
Product ID 0025-1381_30a6488d-0471-4a93-8426-afd35a105254
Description

100 TABLET, FILM COATED in 1 BOTTLE (0025-1381-31)

Marketing

Marketing Status
Discontinued 2026-04-30
Brand daypro
Generic oxaprozin
Sample Package No

Linked Drug Pages (1)

Daypro ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "30a6488d-0471-4a93-8426-afd35a105254", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0300251381317"], "unii": ["MHJ80W9LRB"], "rxcui": ["207243", "312132"], "spl_set_id": ["ea1de47e-3101-4414-817c-0a098af8988c"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0025-1381-31)", "package_ndc": "0025-1381-31", "marketing_end_date": "20260430", "marketing_start_date": "19921029"}], "brand_name": "Daypro", "product_id": "0025-1381_30a6488d-0471-4a93-8426-afd35a105254", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0025-1381", "generic_name": "oxaprozin", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Daypro", "active_ingredients": [{"name": "OXAPROZIN", "strength": "600 mg/1"}], "application_number": "NDA018841", "marketing_category": "NDA", "marketing_end_date": "20260430", "marketing_start_date": "19921029"}