Package 82804-261-60

Brand: oxaprozin

Generic: oxaprozin
NDC Package

Package Facts

Identity

Package NDC 82804-261-60
Digits Only 8280426160
Product NDC 82804-261
Description

60 TABLET, FILM COATED in 1 BOTTLE (82804-261-60)

Marketing

Marketing Status
Marketed Since 2025-12-12
Brand oxaprozin
Generic oxaprozin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3fbea8c-bc0d-4dcd-a14e-a4575dceeea6", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0382804261604"], "unii": ["MHJ80W9LRB"], "rxcui": ["312132"], "spl_set_id": ["e3fbea8c-bc0d-4dcd-a14e-a4575dceeea6"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (82804-261-60)", "package_ndc": "82804-261-60", "marketing_start_date": "20251212"}], "brand_name": "Oxaprozin", "product_id": "82804-261_e3fbea8c-bc0d-4dcd-a14e-a4575dceeea6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "82804-261", "generic_name": "Oxaprozin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaprozin", "active_ingredients": [{"name": "OXAPROZIN", "strength": "600 mg/1"}], "application_number": "ANDA075855", "marketing_category": "ANDA", "marketing_start_date": "20010131", "listing_expiration_date": "20261231"}