Package 70518-3431-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 70518-3431-0
Digits Only 7051834310
Product NDC 70518-3431
Product ID 70518-3431_409402a6-461c-044b-e063-6294a90ac7da
Description

60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3431-0)

Marketing

Marketing Status
Marketed Since 2022-06-03
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": "409402a6-461c-044b-e063-6294a90ac7da", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["bb94bbb1-07c1-49be-8c2c-f5635c65366d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3431-0)", "package_ndc": "70518-3431-0", "marketing_start_date": "20220603"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-3431-2)  / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3431-3)", "package_ndc": "70518-3431-2", "marketing_start_date": "20220628"}], "brand_name": "Divalproex Sodium", "product_id": "70518-3431_409402a6-461c-044b-e063-6294a90ac7da", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-3431", "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": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20220603", "listing_expiration_date": "20261231"}