Package 11673-569-03

{"route": ["TOPICAL"], "spl_id": "3f9d13e9-6d6c-41cd-b2ba-9567247172eb", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["0b7ae58c-cdaf-4343-a199-7a90bf901eb5"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (11673-569-01)  / 100 g in 1 TUBE", "package_ndc": "11673-569-01", "marketing_start_date": "20200819"}, {"sample": false, "description": "1 TUBE in 1 CARTON (11673-569-03)  / 150 g in 1 TUBE", "package_ndc": "11673-569-03", "marketing_start_date": "20210318"}], "brand_name": "up and up arthritis pain reliever", "product_id": "11673-569_3f9d13e9-6d6c-41cd-b2ba-9567247172eb", "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": "11673-569", "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": "20200819", "listing_expiration_date": "20261231"}