Package 80425-0569-1

{"route": ["ORAL"], "spl_id": "47a7a66e-0806-6ab3-e063-6394a90a9406", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["47a7a294-55bb-8d19-e063-6394a90a5440"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (80425-0569-1)", "package_ndc": "80425-0569-1", "marketing_start_date": "20260105"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (80425-0569-2)", "package_ndc": "80425-0569-2", "marketing_start_date": "20260105"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "80425-0569_47a7a66e-0806-6ab3-e063-6394a90a9406", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0569", "generic_name": "Diclofenac Sodium", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "20251231", "listing_expiration_date": "20271231"}