Package 70518-4553-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 70518-4553-0
Digits Only 7051845530
Product NDC 70518-4553
Product ID 70518-4553_48ec8832-fd78-6931-e063-6294a90a7063
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4553-0)

Marketing

Marketing Status
Marketed Since 2026-01-21
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48ec8832-fd78-6931-e063-6294a90a7063", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["d48af379-bd5d-48e1-ad2d-86c493d9cbea"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4553-0)", "package_ndc": "70518-4553-0", "marketing_start_date": "20260121"}], "brand_name": "divalproex sodium", "product_id": "70518-4553_48ec8832-fd78-6931-e063-6294a90a7063", "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": "70518-4553", "generic_name": "divalproex sodium", "labeler_name": "REMEDYREPACK INC.", "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": "20260121", "listing_expiration_date": "20271231"}