Package 71335-2344-1

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2344-1
Digits Only 7133523441
Product NDC 71335-2344
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-1)

Marketing

Marketing Status
Marketed Since 2024-05-30
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": "d41d8bda-5623-4398-afb2-2a4a3d6dd0f1", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["48a6e47a-3697-492d-9086-56e4ca0151e5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-1)", "package_ndc": "71335-2344-1", "marketing_start_date": "20240530"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-2)", "package_ndc": "71335-2344-2", "marketing_start_date": "20240530"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-3)", "package_ndc": "71335-2344-3", "marketing_start_date": "20240129"}, {"sample": false, "description": "180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-4)", "package_ndc": "71335-2344-4", "marketing_start_date": "20240530"}, {"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-5)", "package_ndc": "71335-2344-5", "marketing_start_date": "20240530"}], "brand_name": "Divalproex Sodium", "product_id": "71335-2344_d41d8bda-5623-4398-afb2-2a4a3d6dd0f1", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-2344", "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": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}