Package 16571-842-10

{"route": ["ORAL"], "spl_id": "1e184d68-6ad3-484c-9b26-dc835ed91cbb", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["947c11ca-ca0c-42df-8cc5-3db06458ca5b"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-842-01)", "package_ndc": "16571-842-01", "marketing_start_date": "20250213"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-842-10)", "package_ndc": "16571-842-10", "marketing_start_date": "20250918"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-842-50)", "package_ndc": "16571-842-50", "marketing_start_date": "20250213"}], "brand_name": "POTASSIUM CHLORIDE EXTENDED RELEASE", "product_id": "16571-842_1e184d68-6ad3-484c-9b26-dc835ed91cbb", "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": "16571-842", "generic_name": "potassium chloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE EXTENDED RELEASE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA217412", "marketing_category": "ANDA", "marketing_start_date": "20250213", "listing_expiration_date": "20271231"}