Package 51672-4243-9

{"route": ["ORAL"], "spl_id": "3b8ff35a-8b5e-7aca-e063-6394a90aea34", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "unii": ["9U7D5QH5AE"], "rxcui": ["391937"], "spl_set_id": ["391cfd01-c1fa-41f9-abd7-d0abe9a27634"], "pharm_class_pe": ["Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Osmotic Laxative [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]", "Acidifying Activity [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-4243-9)  / 473 mL in 1 BOTTLE", "package_ndc": "51672-4243-9", "marketing_start_date": "20250602"}], "brand_name": "Lactulose", "product_id": "51672-4243_3b8ff35a-8b5e-7aca-e063-6394a90aea34", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "51672-4243", "generic_name": "Lactulose", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lactulose", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/15mL"}], "application_number": "ANDA218858", "marketing_category": "ANDA", "marketing_start_date": "20250602", "listing_expiration_date": "20261231"}