Package 81033-005-01

{"route": ["ORAL"], "spl_id": "42df2224-eb9a-e3a5-e063-6394a90aa5c7", "openfda": {"unii": ["5QB0T2IUN0", "NBZ3QY004S"], "rxcui": ["243463"], "spl_set_id": ["42df2198-14dc-da1c-e063-6394a90a1ae6"], "manufacturer_name": ["Kesin Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-005-01)  / 30 mL in 1 CUP, UNIT-DOSE (81033-005-30)", "package_ndc": "81033-005-01", "marketing_start_date": "20251105"}], "brand_name": "Kesin MAG-AL", "product_id": "81033-005_42df2224-eb9a-e3a5-e063-6394a90aa5c7", "dosage_form": "SUSPENSION", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "81033-005", "generic_name": "Aluminum and Magnesium Hydroxide Suspension", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kesin MAG-AL", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "200 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "200 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251105", "listing_expiration_date": "20261231"}