Package 68001-566-00

{"route": ["ORAL"], "spl_id": "4341146a-910b-db91-e063-6394a90af245", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["d605ca36-2bfa-42cb-a46c-8ecb3162994e"], "manufacturer_name": ["Bluepoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-566-00)", "package_ndc": "68001-566-00", "marketing_start_date": "20230417"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68001-566-03)", "package_ndc": "68001-566-03", "marketing_start_date": "20230417"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "68001-566_4341146a-910b-db91-e063-6394a90af245", "dosage_form": "TABLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "68001-566", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Bluepoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20210130", "listing_expiration_date": "20261231"}