Package 50090-5361-0

{"route": ["ORAL"], "spl_id": "7becc541-9068-4c11-9211-e000b9e57ee6", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["517d6b02-0e68-4d6b-98b3-eac0be457e6b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-0)", "package_ndc": "50090-5361-0", "marketing_start_date": "20201113"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-1)", "package_ndc": "50090-5361-1", "marketing_start_date": "20201113"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-2)", "package_ndc": "50090-5361-2", "marketing_start_date": "20201113"}], "brand_name": "Pantoprazole Sodium", "product_id": "50090-5361_7becc541-9068-4c11-9211-e000b9e57ee6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-5361", "generic_name": "Pantoprazole Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20120928", "listing_expiration_date": "20261231"}