Package 68001-647-00

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 68001-647-00
Digits Only 6800164700
Product NDC 68001-647
Product ID 68001-647_3ff10d5a-070e-fc82-e063-6394a90a161f
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-647-00)

Marketing

Marketing Status
Marketed Since 2025-08-06
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (1)

divalproex sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ff10d5a-070e-fc82-e063-6394a90a161f", "openfda": {"upc": ["0368001647007", "0368001646000"], "unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["352b4c3c-e419-4827-9e00-febb0164e0f5"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-647-00)", "package_ndc": "68001-647-00", "marketing_start_date": "20250806"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-647-03)", "package_ndc": "68001-647-03", "marketing_start_date": "20250806"}], "brand_name": "divalproex sodium", "product_id": "68001-647_3ff10d5a-070e-fc82-e063-6394a90a161f", "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": "68001-647", "generic_name": "divalproex sodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA214643", "marketing_category": "ANDA", "marketing_start_date": "20250606", "listing_expiration_date": "20261231"}