Package 47335-308-13

{"route": ["ORAL"], "spl_id": "4a5c474b-e752-4d01-be37-a66e7c9bf62e", "openfda": {"upc": ["0347335307887", "0347335308884"], "unii": ["WY6W63843K"], "rxcui": ["854880", "854894"], "spl_set_id": ["0c64bc71-2e7f-4b15-a8e1-acb8de04395f"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-308-13)", "package_ndc": "47335-308-13", "marketing_start_date": "20170515"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-308-88)", "package_ndc": "47335-308-88", "marketing_start_date": "20170515"}], "brand_name": "Zolpidem Tartrate", "product_id": "47335-308_4a5c474b-e752-4d01-be37-a66e7c9bf62e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Agonists [MoA]", "Pyridines [CS]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "47335-308", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem Tartrate", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "12.5 mg/1"}], "application_number": "ANDA204170", "marketing_category": "ANDA", "marketing_start_date": "20170515", "listing_expiration_date": "20261231"}