Package 50228-421-01

{"route": ["ORAL"], "spl_id": "08a26093-1715-5580-e063-6294a90a4ff6", "openfda": {"upc": ["0350228421102", "0350228420105", "0350228420303", "0350228421010", "0350228420013", "0350228421300"], "unii": ["I9W7N6B1KJ"], "rxcui": ["248642", "313990"], "spl_set_id": ["b5035f61-693e-4386-8a07-3c36a6a46917"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50228-421-01)", "package_ndc": "50228-421-01", "marketing_start_date": "20190320"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (50228-421-10)", "package_ndc": "50228-421-10", "marketing_start_date": "20190320"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50228-421-30)", "package_ndc": "50228-421-30", "marketing_start_date": "20190320"}], "brand_name": "Fluoxetine", "product_id": "50228-421_08a26093-1715-5580-e063-6294a90a4ff6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50228-421", "generic_name": "Fluoxetine", "labeler_name": "ScieGen Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA210935", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}