Package 68788-8262-3

{"route": ["ORAL"], "spl_id": "8b2ffdb0-2cd6-4ccf-8bbe-6d61c4b7720d", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["3f19ed0e-6c73-482c-94d6-d3205318fd6f"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8262-3)", "package_ndc": "68788-8262-3", "marketing_start_date": "20220919"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8262-6)", "package_ndc": "68788-8262-6", "marketing_start_date": "20220919"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8262-9)", "package_ndc": "68788-8262-9", "marketing_start_date": "20220919"}], "brand_name": "Potassium Chloride", "product_id": "68788-8262_8b2ffdb0-2cd6-4ccf-8bbe-6d61c4b7720d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "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": "68788-8262", "generic_name": "Potassium Chloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20220919", "listing_expiration_date": "20261231"}