Package 72888-075-00

{"route": ["ORAL"], "spl_id": "43ef4dac-5602-40dc-e063-6394a90af863", "openfda": {"upc": ["0372888076058", "0372888201009", "0372888075006", "0372888201016", "0372888075051", "0372888076010", "0372888075013"], "unii": ["660YQ98I10"], "rxcui": ["198116", "628953", "2693253"], "spl_set_id": ["8000e242-fe20-4d02-8f7d-97298857cf4c"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-075-00)", "package_ndc": "72888-075-00", "marketing_start_date": "20220725"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-075-01)", "package_ndc": "72888-075-01", "marketing_start_date": "20220725"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-075-05)", "package_ndc": "72888-075-05", "marketing_start_date": "20220725"}], "brand_name": "Potassium chloride", "product_id": "72888-075_43ef4dac-5602-40dc-e063-6394a90af863", "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": "72888-075", "generic_name": "Potassium Chloride", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA215725", "marketing_category": "ANDA", "marketing_start_date": "20220725", "listing_expiration_date": "20261231"}