Package 43547-550-50

{"route": ["ORAL"], "spl_id": "f704b746-ab75-4484-8704-5baa94a07750", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["403888", "1801294", "1801298"], "spl_set_id": ["f704b746-ab75-4484-8704-5baa94a07750"], "manufacturer_name": ["Solco Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43547-550-10)", "package_ndc": "43547-550-10", "marketing_start_date": "20190430"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (43547-550-11)", "package_ndc": "43547-550-11", "marketing_start_date": "20190430"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (43547-550-50)", "package_ndc": "43547-550-50", "marketing_start_date": "20190430"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "43547-550_f704b746-ab75-4484-8704-5baa94a07750", "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": "43547-550", "generic_name": "potassium chloride extended-release", "labeler_name": "Solco Healthcare LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA209922", "marketing_category": "ANDA", "marketing_start_date": "20190430", "listing_expiration_date": "20261231"}