Package 50090-6074-0

{"route": ["ORAL"], "spl_id": "9e7a58a5-0a83-4cb0-9dce-b138cf6d488e", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["3df910c5-b6f0-4a65-9640-b702ecea49f9"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6074-0)", "package_ndc": "50090-6074-0", "marketing_start_date": "20220914"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6074-1)", "package_ndc": "50090-6074-1", "marketing_start_date": "20220914"}], "brand_name": "Divalproex sodium", "product_id": "50090-6074_9e7a58a5-0a83-4cb0-9dce-b138cf6d488e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "50090-6074", "generic_name": "Divalproex sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA202419", "marketing_category": "ANDA", "marketing_start_date": "20140602", "listing_expiration_date": "20261231"}