Package 70518-4557-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 70518-4557-0
Digits Only 7051845570
Product NDC 70518-4557
Product ID 70518-4557_49646ced-d52b-dab7-e063-6294a90aba3f
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4557-0)

Marketing

Marketing Status
Marketed Since 2026-01-27
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": "49646ced-d52b-dab7-e063-6294a90aba3f", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563"], "spl_set_id": ["93d6ddb5-7143-4917-baf7-31cbf8a90e8d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4557-0)", "package_ndc": "70518-4557-0", "marketing_start_date": "20260127"}], "brand_name": "divalproex sodium", "product_id": "70518-4557_49646ced-d52b-dab7-e063-6294a90aba3f", "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": "70518-4557", "generic_name": "divalproex sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA214643", "marketing_category": "ANDA", "marketing_start_date": "20260127", "listing_expiration_date": "20271231"}