Package 71335-2277-1

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2277-1
Digits Only 7133522771
Product NDC 71335-2277
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-1)

Marketing

Marketing Status
Marketed Since 2023-11-29
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": "ac3ae02b-9b59-4a0a-9610-b2bfec83ac15", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["cd6fe37a-d26d-4ae8-a894-b44878e6bf8e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-1)", "package_ndc": "71335-2277-1", "marketing_start_date": "20231129"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-2)", "package_ndc": "71335-2277-2", "marketing_start_date": "20240530"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-3)", "package_ndc": "71335-2277-3", "marketing_start_date": "20240530"}, {"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-4)", "package_ndc": "71335-2277-4", "marketing_start_date": "20240530"}], "brand_name": "Divalproex Sodium", "product_id": "71335-2277_ac3ae02b-9b59-4a0a-9610-b2bfec83ac15", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71335-2277", "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"}