Package 72189-648-04

{"route": ["ORAL"], "spl_id": "44821394-e7a8-de9d-e063-6294a90a97b9", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["42c92fcc-21d2-d32a-e063-6294a90a8312"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-04)", "package_ndc": "72189-648-04", "marketing_start_date": "20251104"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-30)", "package_ndc": "72189-648-30", "marketing_start_date": "20251104"}], "brand_name": "Potassium Chloride ER", "product_id": "72189-648_44821394-e7a8-de9d-e063-6294a90a97b9", "dosage_form": "TABLET, 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": "72189-648", "generic_name": "Potassium Chloride ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride ER", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20251104", "listing_expiration_date": "20261231"}