Package 60760-698-60

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 60760-698-60
Digits Only 6076069860
Product NDC 60760-698
Product ID 60760-698_35a91dd3-19d1-09cb-e063-6394a90af01b
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-698-60)

Marketing

Marketing Status
Marketed Since 2025-05-13
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": "35a91dd3-19d1-09cb-e063-6394a90af01b", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["35a91dd3-19d0-09cb-e063-6394a90af01b"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-698-60)", "package_ndc": "60760-698-60", "marketing_start_date": "20250513"}], "brand_name": "Divalproex Sodium", "product_id": "60760-698_35a91dd3-19d1-09cb-e063-6394a90af01b", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "60760-698", "generic_name": "Divalproex Sodium", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_start_date": "20141024", "listing_expiration_date": "20261231"}