Package 68788-8099-3

{"route": ["ORAL"], "spl_id": "b29d7b77-d758-4b93-bf05-76cf2632d9cc", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["94642db1-5c75-44c4-92b4-8385b486df82"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8099-3)", "package_ndc": "68788-8099-3", "marketing_start_date": "20211006"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8099-6)", "package_ndc": "68788-8099-6", "marketing_start_date": "20211006"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8099-9)", "package_ndc": "68788-8099-9", "marketing_start_date": "20211006"}], "brand_name": "Montelukast", "product_id": "68788-8099_b29d7b77-d758-4b93-bf05-76cf2632d9cc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68788-8099", "generic_name": "Montelukast", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA202843", "marketing_category": "ANDA", "marketing_start_date": "20211006", "listing_expiration_date": "20261231"}