Package 47335-922-82

{"route": ["ORAL"], "spl_id": "506a57ae-8168-44b2-88ef-b9f0e4d0c6b9", "openfda": {"nui": ["N0000008486"], "upc": ["0347335943863", "0347335980868"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809992", "809996", "810000"], "spl_set_id": ["2098d3a5-776e-4b52-8ade-80a3ab7b3de7"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (47335-922-18)", "package_ndc": "47335-922-18", "marketing_start_date": "20220319"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (47335-922-82)", "package_ndc": "47335-922-82", "marketing_start_date": "20220319"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (47335-922-86)", "package_ndc": "47335-922-86", "marketing_start_date": "20220319"}], "brand_name": "Lacosamide", "product_id": "47335-922_506a57ae-8168-44b2-88ef-b9f0e4d0c6b9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "47335-922", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "100 mg/1"}], "application_number": "ANDA205031", "marketing_category": "ANDA", "marketing_start_date": "20220319", "listing_expiration_date": "20261231"}