Package 70000-0436-1

{"route": ["ORAL"], "spl_id": "dcfb5e7e-1314-4bf0-aaf0-a2c76dce42e7", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["eab5a905-67fb-494e-8f55-aeeab4c2dce2"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC. DBA LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (70000-0436-1)", "package_ndc": "70000-0436-1", "marketing_end_date": "20270930", "marketing_start_date": "20190710"}], "brand_name": "Leader Ultra Strength Antacid", "product_id": "70000-0436_dcfb5e7e-1314-4bf0-aaf0-a2c76dce42e7", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "70000-0436", "generic_name": "Calcium carbonate", "labeler_name": "CARDINAL HEALTH 110, LLC. DBA LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Leader Ultra Strength Antacid", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270930", "marketing_start_date": "20190710"}