Package 72189-462-30

{"route": ["ORAL"], "spl_id": "2c4ddf50-4e21-7c59-e063-6294a90ace41", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["f988aa11-60ef-411e-e053-6294a90a522a"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-462-30)", "package_ndc": "72189-462-30", "marketing_start_date": "20230417"}], "brand_name": "Potassium Chloride ER", "product_id": "72189-462_2c4ddf50-4e21-7c59-e063-6294a90ace41", "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": "72189-462", "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": "ANDA203562", "marketing_category": "ANDA", "marketing_start_date": "20230417", "listing_expiration_date": "20261231"}