Package 72162-2515-1

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 72162-2515-1
Digits Only 7216225151
Product NDC 72162-2515
Product ID 72162-2515_374e53c6-3037-f8e5-e063-6394a90a07ef
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2515-1)

Marketing

Marketing Status
Marketed Since 2025-06-09
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": "374e53c6-3037-f8e5-e063-6394a90a07ef", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563"], "spl_set_id": ["8b3cb30a-8d81-4aa9-bdb4-19413ae5fedf"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2515-1)", "package_ndc": "72162-2515-1", "marketing_start_date": "20250609"}], "brand_name": "Divalproex sodium", "product_id": "72162-2515_374e53c6-3037-f8e5-e063-6394a90a07ef", "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": "72162-2515", "generic_name": "Divalproex sodium", "labeler_name": "Bryant Ranch Prepack", "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": "20140602", "listing_expiration_date": "20261231"}