Package 72189-636-60

Brand: divalproex sodium d/r

Generic: divalproex sodium d/r
NDC Package

Package Facts

Identity

Package NDC 72189-636-60
Digits Only 7218963660
Product NDC 72189-636
Product ID 72189-636_3aff8f08-d8e9-cd13-e063-6394a90aa00c
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-636-60)

Marketing

Marketing Status
Marketed Since 2025-07-28
Brand divalproex sodium d/r
Generic divalproex sodium d/r
Sample Package No

Linked Drug Pages (1)

Divalproex Sodium D/R ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3aff8f08-d8e9-cd13-e063-6394a90aa00c", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["3aff8f08-d8e8-cd13-e063-6394a90aa00c"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-636-60)", "package_ndc": "72189-636-60", "marketing_start_date": "20250728"}], "brand_name": "Divalproex Sodium D/R", "product_id": "72189-636_3aff8f08-d8e9-cd13-e063-6394a90aa00c", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72189-636", "generic_name": "Divalproex Sodium D/R", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium D/R", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20250728", "listing_expiration_date": "20261231"}