Package 67046-1647-3

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 67046-1647-3
Digits Only 6704616473
Product NDC 67046-1647
Product ID 67046-1647_4834727a-982f-9ba7-e063-6394a90a8180
Description

30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1647-3)

Marketing

Marketing Status
Marketed Since 2024-06-26
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": "4834727a-982f-9ba7-e063-6394a90a8180", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["4834732f-6044-946c-e063-6394a90a5da3"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1647-3)", "package_ndc": "67046-1647-3", "marketing_start_date": "20240626"}], "brand_name": "divalproex sodium", "product_id": "67046-1647_4834727a-982f-9ba7-e063-6394a90a8180", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "67046-1647", "generic_name": "divalproex sodium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA078853", "marketing_category": "ANDA", "marketing_start_date": "20240626", "listing_expiration_date": "20271231"}