Package 70518-1781-1

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 70518-1781-1
Digits Only 7051817811
Product NDC 70518-1781
Product ID 70518-1781_49749aa6-a0ec-cf8f-e063-6394a90a1129
Description

100 POUCH in 1 BOX (70518-1781-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-1781-2)

Marketing

Marketing Status
Marketed Since 2020-08-03
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": "49749aa6-a0ec-cf8f-e063-6394a90a1129", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563"], "spl_set_id": ["7e96b724-5f5f-43cb-8d8b-adff3e1fc779"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-1781-1)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-1781-2)", "package_ndc": "70518-1781-1", "marketing_start_date": "20200803"}], "brand_name": "Divalproex sodium", "product_id": "70518-1781_49749aa6-a0ec-cf8f-e063-6394a90a1129", "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": "70518-1781", "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": "ANDA202419", "marketing_category": "ANDA", "marketing_start_date": "20190107", "listing_expiration_date": "20271231"}