Package 70518-4050-0

{"route": ["ORAL"], "spl_id": "3fa16c36-fa12-db93-e063-6394a90ad2bf", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["f75713cf-6902-4160-94cb-335a1ecdbbbe"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-4050-0)", "package_ndc": "70518-4050-0", "marketing_start_date": "20240411"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-4050-1)  / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-4050-2)", "package_ndc": "70518-4050-1", "marketing_start_date": "20240615"}], "brand_name": "Potassium Chloride", "product_id": "70518-4050_3fa16c36-fa12-db93-e063-6394a90ad2bf", "dosage_form": "CAPSULE, 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": "70518-4050", "generic_name": "Potassium Chloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214686", "marketing_category": "ANDA", "marketing_start_date": "20240411", "listing_expiration_date": "20261231"}