Package 24979-230-00

{"route": ["ORAL"], "spl_id": "d03706f3-78e7-4be3-8f41-af67f60b0178", "openfda": {"upc": ["0324979229010", "0324979230016"], "unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["a230185f-5493-487d-892a-5219869b4e47"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "64000 TABLET, EXTENDED RELEASE in 1 DRUM (24979-230-00)", "package_ndc": "24979-230-00", "marketing_start_date": "20250601"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-01)", "package_ndc": "24979-230-01", "marketing_start_date": "20241028"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-03)", "package_ndc": "24979-230-03", "marketing_start_date": "20241028"}], "brand_name": "Potassium Chloride", "product_id": "24979-230_d03706f3-78e7-4be3-8f41-af67f60b0178", "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": "24979-230", "generic_name": "Potassium Chloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA218979", "marketing_category": "ANDA", "marketing_start_date": "20241028", "listing_expiration_date": "20261231"}