Package 82442-251-01

{"route": ["TOPICAL"], "spl_id": "14f54267-fa3d-4ffc-a197-1cf8b02ac17c", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["3a9b32af-a3cd-496b-9698-0421443e0385"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (82442-251-01)  / 100 g in 1 TUBE", "package_ndc": "82442-251-01", "marketing_start_date": "20250827"}, {"sample": false, "description": "1 TUBE in 1 CARTON (82442-251-03)  / 150 g in 1 TUBE", "package_ndc": "82442-251-03", "marketing_start_date": "20250827"}], "brand_name": "UP AND UP ARTHRITIS PAIN RELIEVER", "product_id": "82442-251_14f54267-fa3d-4ffc-a197-1cf8b02ac17c", "dosage_form": "GEL", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "82442-251", "generic_name": "DICLOFENAC SODIUM", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "UP AND UP ARTHRITIS PAIN RELIEVER", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA211253", "marketing_category": "ANDA", "marketing_start_date": "20250827", "listing_expiration_date": "20261231"}