Package 80425-0552-1

{"route": ["ORAL"], "spl_id": "4136d849-f075-057c-e063-6394a90a91f1", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["4136d983-75fa-9604-e063-6294a90aaac6"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0552-1)", "package_ndc": "80425-0552-1", "marketing_start_date": "20251015"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0552-2)", "package_ndc": "80425-0552-2", "marketing_start_date": "20251015"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0552-3)", "package_ndc": "80425-0552-3", "marketing_start_date": "20251015"}], "brand_name": "Pantoprazole", "product_id": "80425-0552_4136d849-f075-057c-e063-6394a90a91f1", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "80425-0552", "generic_name": "Pantoprazole", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA077619", "marketing_category": "ANDA", "marketing_start_date": "20251015", "listing_expiration_date": "20261231"}