Package 71335-2782-5

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2782-5
Digits Only 7133527825
Product NDC 71335-2782
Description

120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-5)

Marketing

Marketing Status
Marketed Since 2025-09-24
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "059c400c-3e48-4eda-957a-3881b9907ddf", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["df8f3825-a037-4343-859d-e59bca5f1e43"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-1)", "package_ndc": "71335-2782-1", "marketing_start_date": "20250924"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-2)", "package_ndc": "71335-2782-2", "marketing_start_date": "20250924"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-3)", "package_ndc": "71335-2782-3", "marketing_start_date": "20250924"}, {"sample": false, "description": "180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-4)", "package_ndc": "71335-2782-4", "marketing_start_date": "20250924"}, {"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-5)", "package_ndc": "71335-2782-5", "marketing_start_date": "20250924"}], "brand_name": "divalproex sodium", "product_id": "71335-2782_059c400c-3e48-4eda-957a-3881b9907ddf", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-2782", "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": "500 mg/1"}], "application_number": "ANDA078853", "marketing_category": "ANDA", "marketing_start_date": "20240626", "listing_expiration_date": "20261231"}