Package 62756-796-08

{"route": ["ORAL"], "spl_id": "044ee7fd-d980-4b48-b2b7-aa1717e44638", "openfda": {"upc": ["0362756796836", "0362756798830"], "unii": ["644VL95AO6"], "rxcui": ["1099625", "1099678", "1099870"], "spl_set_id": ["64797788-fdcb-4d12-a1a4-743ad71bd17b"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-08)", "package_ndc": "62756-796-08", "marketing_start_date": "20080729"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-13)", "package_ndc": "62756-796-13", "marketing_start_date": "20080729"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-18)", "package_ndc": "62756-796-18", "marketing_start_date": "20080729"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-83)", "package_ndc": "62756-796-83", "marketing_start_date": "20080729"}, {"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-88)", "package_ndc": "62756-796-88", "marketing_start_date": "20080729"}], "brand_name": "Divalproex Sodium", "product_id": "62756-796_044ee7fd-d980-4b48-b2b7-aa1717e44638", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "62756-796", "generic_name": "Divalproex Sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}