Package 72189-629-30

{"route": ["ORAL"], "spl_id": "377854ff-8035-c7ac-e063-6294a90a0817", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["377854ff-8034-c7ac-e063-6294a90a0817"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-629-30)", "package_ndc": "72189-629-30", "marketing_start_date": "20250613"}], "brand_name": "Potassium Chloride ER", "product_id": "72189-629_377854ff-8035-c7ac-e063-6294a90a0817", "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": "72189-629", "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": "1500 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20250613", "listing_expiration_date": "20261231"}