Package 24979-232-02

{"route": ["ORAL"], "spl_id": "70a9e07c-81ba-42a4-ae82-5f0125673744", "openfda": {"upc": ["0324979231020", "0324979231013", "0324979232010"], "unii": ["660YQ98I10"], "rxcui": ["198116", "628953"], "spl_set_id": ["02707146-331f-4511-a187-0152fc8bca85"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-232-01)", "package_ndc": "24979-232-01", "marketing_start_date": "20230410"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-232-02)", "package_ndc": "24979-232-02", "marketing_start_date": "20230410"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "24979-232_70a9e07c-81ba-42a4-ae82-5f0125673744", "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": "24979-232", "generic_name": "Potassium Chloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA209688", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}