Package 72162-2316-1

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 72162-2316-1
Digits Only 7216223161
Product NDC 72162-2316
Product ID 72162-2316_76973fa3-9fc8-4422-9002-5a632c98c881
Description

100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-1)

Marketing

Marketing Status
Marketed Since 2024-05-16
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": "76973fa3-9fc8-4422-9002-5a632c98c881", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["47412563-ec3e-44fd-9f3f-c00b9b09033a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-1)", "package_ndc": "72162-2316-1", "marketing_start_date": "20240516"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-5)", "package_ndc": "72162-2316-5", "marketing_start_date": "20240516"}], "brand_name": "Divalproex Sodium", "product_id": "72162-2316_76973fa3-9fc8-4422-9002-5a632c98c881", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72162-2316", "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": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}