Package 70518-2964-4

{"route": ["ORAL"], "spl_id": "4aba2fbf-fcb8-040b-e063-6394a90a3ba3", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["16c775e4-0dd8-4e9f-b2bf-dd2b639374cf"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2964-0)", "package_ndc": "70518-2964-0", "marketing_start_date": "20201209"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2964-3)", "package_ndc": "70518-2964-3", "marketing_start_date": "20240312"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2964-4)", "package_ndc": "70518-2964-4", "marketing_start_date": "20250325"}], "brand_name": "Potassium Chloride", "product_id": "70518-2964_4aba2fbf-fcb8-040b-e063-6394a90a3ba3", "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": "70518-2964", "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": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20201209", "listing_expiration_date": "20271231"}