Package 62332-821-31

{"route": ["ORAL"], "spl_id": "ea4c67a5-e435-49c1-bba6-6822dc63e167", "openfda": {"upc": ["0362332821716", "0362332821310"], "unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["fea19b14-d8ed-4954-bc54-b9240f78b3c3"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (62332-821-10)  / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "62332-821-10", "marketing_start_date": "20241223"}, {"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-31)", "package_ndc": "62332-821-31", "marketing_start_date": "20241223"}, {"sample": false, "description": "500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-71)", "package_ndc": "62332-821-71", "marketing_start_date": "20250321"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-91)", "package_ndc": "62332-821-91", "marketing_start_date": "20241223"}], "brand_name": "Divalproex sodium", "product_id": "62332-821_ea4c67a5-e435-49c1-bba6-6822dc63e167", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "62332-821", "generic_name": "Divalproex sodium", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA218793", "marketing_category": "ANDA", "marketing_start_date": "20241223", "listing_expiration_date": "20261231"}