Package 24286-1537-7

{"route": ["ORAL"], "spl_id": "47d4f7e8-3e03-1192-e063-6294a90aa739", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1488624"], "spl_set_id": ["fc469943-9749-45ee-93f7-90fdbcdc7215"], "manufacturer_name": ["DLC Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "113 g in 1 BOTTLE, PLASTIC (24286-1537-7)", "package_ndc": "24286-1537-7", "marketing_start_date": "20130925"}, {"sample": false, "description": "226 g in 1 BOTTLE, PLASTIC (24286-1537-8)", "package_ndc": "24286-1537-8", "marketing_start_date": "20190722"}], "brand_name": "DE LA CRUZ SODIUM BICARBONATE ANTACID", "product_id": "24286-1537_47d4f7e8-3e03-1192-e063-6294a90aa739", "dosage_form": "POWDER", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "24286-1537", "generic_name": "SODIUM BICARBONATE", "labeler_name": "DLC Laboratories, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DE LA CRUZ SODIUM BICARBONATE ANTACID", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "2.6 g/2.6g"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130925", "listing_expiration_date": "20271231"}