Package 55154-4679-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 55154-4679-0
Digits Only 5515446790
Product NDC 55154-4679
Product ID 55154-4679_aae490e3-adff-41cc-ad39-488f5449f7b6
Description

10 BLISTER PACK in 1 BAG (55154-4679-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-06-30
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": "aae490e3-adff-41cc-ad39-488f5449f7b6", "openfda": {"upc": ["0055154467902", "0055154714501"], "unii": ["644VL95AO6"], "rxcui": ["1099678", "1099870"], "spl_set_id": ["ee2e8924-2379-400d-9895-e3aa02fe6426"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-4679-0)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-4679-0", "marketing_end_date": "20260630", "marketing_start_date": "20160126"}], "brand_name": "Divalproex Sodium", "product_id": "55154-4679_aae490e3-adff-41cc-ad39-488f5449f7b6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55154-4679", "generic_name": "Divalproex Sodium", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20160126"}