Package 60219-1617-3

{"route": ["ORAL"], "spl_id": "21ca4401-7e47-41a4-9e08-96f2c300dbbf", "openfda": {"upc": ["0360219161719", "0360219161733"], "unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["f9965f73-e189-423f-bd10-c4a0ed12b485"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (60219-1617-3)  / 1.58 g in 1 POUCH (60219-1617-1)", "package_ndc": "60219-1617-3", "marketing_start_date": "20231125"}, {"sample": false, "description": "100 POUCH in 1 CARTON (60219-1617-8)  / 1.58 g in 1 POUCH (60219-1617-1)", "package_ndc": "60219-1617-8", "marketing_start_date": "20231125"}], "brand_name": "Potassium Chloride", "product_id": "60219-1617_21ca4401-7e47-41a4-9e08-96f2c300dbbf", "dosage_form": "FOR SOLUTION", "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": "60219-1617", "generic_name": "Potassium Chloride", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.58g"}], "application_number": "ANDA210902", "marketing_category": "ANDA", "marketing_start_date": "20231125", "listing_expiration_date": "20261231"}