Package 70518-4520-0

{"route": ["ORAL"], "spl_id": "441b5173-63fc-cb2e-e063-6294a90a7b9a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["d1e55181-6f85-42c9-922c-808494b6399a"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4520-0)", "package_ndc": "70518-4520-0", "marketing_start_date": "20251121"}], "brand_name": "POTASSIUM CHLORIDE EXTENDED RELEASE", "product_id": "70518-4520_441b5173-63fc-cb2e-e063-6294a90a7b9a", "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": "70518-4520", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE EXTENDED RELEASE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA211797", "marketing_category": "ANDA", "marketing_start_date": "20251121", "listing_expiration_date": "20261231"}