Package 82804-233-30

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 82804-233-30
Digits Only 8280423330
Product NDC 82804-233
Product ID 82804-233_15ffe3d8-d483-4c45-adc4-1cc8a5b68d19
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30)

Marketing

Marketing Status
Marketed Since 2025-08-06
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": "15ffe3d8-d483-4c45-adc4-1cc8a5b68d19", "openfda": {"upc": ["0382804233304"], "unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["15ffe3d8-d483-4c45-adc4-1cc8a5b68d19"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30)", "package_ndc": "82804-233-30", "marketing_start_date": "20250806"}], "brand_name": "divalproex sodium", "product_id": "82804-233_15ffe3d8-d483-4c45-adc4-1cc8a5b68d19", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "82804-233", "generic_name": "divalproex sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA078853", "marketing_category": "ANDA", "marketing_start_date": "20240626", "listing_expiration_date": "20261231"}