Package 85509-1332-6

{"route": ["ORAL"], "spl_id": "43fc6335-4b31-60bc-e063-6294a90a7362", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["43fc6326-cfe6-7d1c-e063-6394a90abc24"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-3)", "package_ndc": "85509-1332-3", "marketing_start_date": "20251120"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-6)", "package_ndc": "85509-1332-6", "marketing_start_date": "20251120"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-9)", "package_ndc": "85509-1332-9", "marketing_start_date": "20251120"}], "brand_name": "Pantoprazole", "product_id": "85509-1332_43fc6335-4b31-60bc-e063-6294a90a7362", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "85509-1332", "generic_name": "Pantoprazole", "labeler_name": "PHOENIX RX 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": "20110119", "listing_expiration_date": "20261231"}