Package 80425-0094-2

{"route": ["ORAL"], "spl_id": "2a993d77-4867-9feb-e063-6294a90ad629", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["b354053c-cb83-79c6-e053-2a95a90afdbe"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0094-1)", "package_ndc": "80425-0094-1", "marketing_start_date": "20180427"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0094-2)", "package_ndc": "80425-0094-2", "marketing_start_date": "20180427"}], "brand_name": "Rabeprazole Sodium DR", "product_id": "80425-0094_2a993d77-4867-9feb-e063-6294a90ad629", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "80425-0094", "generic_name": "Rabeprazole Sodium", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rabeprazole Sodium", "brand_name_suffix": "DR", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA208644", "marketing_category": "ANDA", "marketing_start_date": "20180427", "listing_expiration_date": "20261231"}