Package 68391-033-65

{"route": ["ORAL"], "spl_id": "c7eedcbf-3b07-4cd3-937b-c56d7cc5bc57", "openfda": {"upc": ["0000000000000"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["c7eedcbf-3b07-4cd3-937b-c56d7cc5bc57"], "manufacturer_name": ["BJWC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "265 TABLET, CHEWABLE in 1 BOTTLE (68391-033-65)", "package_ndc": "68391-033-65", "marketing_start_date": "20250317"}], "brand_name": "BERKLEY JENSEN ULTRA STRENGTH", "product_id": "68391-033_c7eedcbf-3b07-4cd3-937b-c56d7cc5bc57", "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": "68391-033", "generic_name": "ANTACID CALCIUM CARBONATE", "labeler_name": "BJWC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BERKLEY JENSEN", "brand_name_suffix": "ULTRA STRENGTH", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250317", "listing_expiration_date": "20261231"}