Package 67046-1571-3

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 67046-1571-3
Digits Only 6704615713
Product NDC 67046-1571
Product ID 67046-1571_38f4e70f-be4f-ae1d-e063-6394a90ae3e9
Description

30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1571-3)

Marketing

Marketing Status
Marketed Since 2025-07-02
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": "38f4e70f-be4f-ae1d-e063-6394a90ae3e9", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["38f4f2fd-400b-ccc4-e063-6294a90a5f41"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1571-3)", "package_ndc": "67046-1571-3", "marketing_start_date": "20250702"}], "brand_name": "Divalproex Sodium", "product_id": "67046-1571_38f4e70f-be4f-ae1d-e063-6394a90ae3e9", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "67046-1571", "generic_name": "Divalproex Sodium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20250702", "listing_expiration_date": "20261231"}