Package 60290-088-05

{"route": ["ORAL"], "spl_id": "4580535c-79b7-68b5-e063-6394a90a38a9", "openfda": {"upc": ["0360290088028", "0360290088042", "0360290088011", "0360290057024"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942", "857702"], "spl_set_id": ["1fa07fbe-3708-4200-b3ff-a920434896b6"], "manufacturer_name": ["Umedica Laboratories USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60290-088-01)", "package_ndc": "60290-088-01", "marketing_start_date": "20240928"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60290-088-02)", "package_ndc": "60290-088-02", "marketing_start_date": "20240928"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (60290-088-03)", "package_ndc": "60290-088-03", "marketing_start_date": "20240928"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60290-088-04)", "package_ndc": "60290-088-04", "marketing_start_date": "20240928"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (60290-088-05)", "package_ndc": "60290-088-05", "marketing_start_date": "20251030"}], "brand_name": "Diclofenac Potassium", "product_id": "60290-088_4580535c-79b7-68b5-e063-6394a90a38a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "60290-088", "generic_name": "Diclofenac Potassium Tablets", "labeler_name": "Umedica Laboratories USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA215750", "marketing_category": "ANDA", "marketing_start_date": "20220512", "listing_expiration_date": "20261231"}