Package 68788-8617-9

{"route": ["ORAL"], "spl_id": "68ee9209-7a6b-4f51-9252-2e22baaa58f4", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["1eeb3123-9e93-4681-8096-800a7c7acf8a"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8617-3)", "package_ndc": "68788-8617-3", "marketing_start_date": "20240328"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8617-6)", "package_ndc": "68788-8617-6", "marketing_start_date": "20240328"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8617-9)", "package_ndc": "68788-8617-9", "marketing_start_date": "20240328"}], "brand_name": "montelukast sodium", "product_id": "68788-8617_68ee9209-7a6b-4f51-9252-2e22baaa58f4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68788-8617", "generic_name": "montelukast sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "montelukast sodium", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA204290", "marketing_category": "ANDA", "marketing_start_date": "20240328", "listing_expiration_date": "20261231"}