Package 62756-538-18

{"route": ["ORAL"], "spl_id": "9f3fe78f-5fa7-48ab-90cc-5c0ba82c1fb2", "openfda": {"nui": ["N0000175740", "M0483511"], "upc": ["0362756538832"], "unii": ["7LJ087RS6F"], "rxcui": ["199206"], "spl_set_id": ["4c851be4-f0d0-4b24-baf9-427ddfc6f7b0"], "pharm_class_cs": ["Benzothiazoles [CS]"], "pharm_class_epc": ["Benzothiazole [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62756-538-18)", "package_ndc": "62756-538-18", "marketing_start_date": "20130618"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62756-538-83)", "package_ndc": "62756-538-83", "marketing_start_date": "20130618"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (62756-538-86)", "package_ndc": "62756-538-86", "marketing_start_date": "20130618"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62756-538-88)", "package_ndc": "62756-538-88", "marketing_start_date": "20130618"}], "brand_name": "Riluzole", "product_id": "62756-538_9f3fe78f-5fa7-48ab-90cc-5c0ba82c1fb2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Benzothiazole [EPC]", "Benzothiazoles [CS]"], "product_ndc": "62756-538", "generic_name": "Riluzole", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Riluzole", "active_ingredients": [{"name": "RILUZOLE", "strength": "50 mg/1"}], "application_number": "ANDA091417", "marketing_category": "ANDA", "marketing_start_date": "20130618", "listing_expiration_date": "20261231"}