Package 50090-7763-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7763-0
Digits Only 5009077630
Product NDC 50090-7763
Product ID 50090-7763_ff1828be-6b93-4a6c-a181-108d018c83ba
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7763-0)

Marketing

Marketing Status
Marketed Since 2025-11-11
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": "ff1828be-6b93-4a6c-a181-108d018c83ba", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["ea5c5e3c-c23f-4ec0-b1ab-6b317f3d2f91"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7763-0)", "package_ndc": "50090-7763-0", "marketing_start_date": "20251111"}, {"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7763-1)", "package_ndc": "50090-7763-1", "marketing_start_date": "20251111"}], "brand_name": "divalproex sodium", "product_id": "50090-7763_ff1828be-6b93-4a6c-a181-108d018c83ba", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "50090-7763", "generic_name": "divalproex sodium", "labeler_name": "A-S Medication Solutions", "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"}