Package 50090-7639-1

{"route": ["ORAL"], "spl_id": "a3f72472-21b1-44b3-9758-e65b4e02c681", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["8757d093-747b-4e97-af6d-4064b16178b2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-0)", "package_ndc": "50090-7639-0", "marketing_start_date": "20250826"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-1)", "package_ndc": "50090-7639-1", "marketing_start_date": "20250826"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-2)", "package_ndc": "50090-7639-2", "marketing_start_date": "20250826"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-3)", "package_ndc": "50090-7639-3", "marketing_start_date": "20250826"}], "brand_name": "Potassium Chloride", "product_id": "50090-7639_a3f72472-21b1-44b3-9758-e65b4e02c681", "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": "50090-7639", "generic_name": "Potassium Chloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "NDA019123", "marketing_category": "NDA", "marketing_start_date": "19860417", "listing_expiration_date": "20261231"}