Package 80425-0406-1

{"route": ["ORAL"], "spl_id": "1c4616ae-982f-d4b6-e063-6294a90a38f6", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["1c46140c-2399-5ca3-e063-6394a90af33b"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0406-1)", "package_ndc": "80425-0406-1", "marketing_start_date": "20240627"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0406-2)", "package_ndc": "80425-0406-2", "marketing_start_date": "20240627"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0406-3)", "package_ndc": "80425-0406-3", "marketing_start_date": "20240627"}], "brand_name": "Pantoprazole Sodium DR", "product_id": "80425-0406_1c4616ae-982f-d4b6-e063-6294a90a38f6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "80425-0406", "generic_name": "Pantoprazole Sodium", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "brand_name_suffix": "DR", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20240627", "listing_expiration_date": "20261231"}