Package 50090-6108-0

{"route": ["ORAL"], "spl_id": "eeb0e0ae-31b8-4954-ac31-de5c082b18eb", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["6741830f-5d90-4066-bc3b-065059bc150d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6108-0)", "package_ndc": "50090-6108-0", "marketing_start_date": "20220928"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6108-1)", "package_ndc": "50090-6108-1", "marketing_start_date": "20220928"}], "brand_name": "Montelukast", "product_id": "50090-6108_eeb0e0ae-31b8-4954-ac31-de5c082b18eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "50090-6108", "generic_name": "Montelukast", "labeler_name": "A-S Medication Solutions", "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": "20140910", "listing_expiration_date": "20261231"}