Package 68788-8610-9

{"route": ["ORAL"], "spl_id": "4770cc7d-0fd7-4992-bd3e-f59c54cbd3b3", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["64a3b181-e8d8-4caf-9f1b-e0063d0bd94a"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8610-3)", "package_ndc": "68788-8610-3", "marketing_start_date": "20240320"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8610-6)", "package_ndc": "68788-8610-6", "marketing_start_date": "20240320"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8610-9)", "package_ndc": "68788-8610-9", "marketing_start_date": "20240320"}], "brand_name": "Montelukast Sodium", "product_id": "68788-8610_4770cc7d-0fd7-4992-bd3e-f59c54cbd3b3", "dosage_form": "TABLET", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "68788-8610", "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": "ANDA201515", "marketing_category": "ANDA", "marketing_start_date": "20240320", "listing_expiration_date": "20261231"}