Package 27241-115-10

{"route": ["ORAL"], "spl_id": "d905fd66-055a-4130-8e67-20c0645362f0", "openfda": {"upc": ["0327241115011"], "unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["773a289b-65ed-4045-80c5-f00e28c1c079"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-01)", "package_ndc": "27241-115-01", "marketing_start_date": "20200515"}, {"sample": false, "description": "500 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-05)", "package_ndc": "27241-115-05", "marketing_start_date": "20200515"}, {"sample": false, "description": "1000 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-10)", "package_ndc": "27241-115-10", "marketing_start_date": "20200515"}], "brand_name": "Divalproex sodium", "product_id": "27241-115_d905fd66-055a-4130-8e67-20c0645362f0", "dosage_form": "CAPSULE, COATED PELLETS", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "27241-115", "generic_name": "Divalproex sodium", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA213181", "marketing_category": "ANDA", "marketing_start_date": "20200515", "listing_expiration_date": "20271231"}