divalproex sodium

Generic: divalproex sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name divalproex sodium
Generic Name divalproex sodium
Labeler a-s medication solutions
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 250 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7763
Product ID 50090-7763_ff1828be-6b93-4a6c-a181-108d018c83ba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078853
Listing Expiration 2026-12-31
Marketing Start 2024-06-26

Pharmacologic Class

Classes
anti-epileptic agent [epc] decreased central nervous system disorganized electrical activity [pe] mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907763
Hyphenated Format 50090-7763

Supplemental Identifiers

RxCUI
1099678
UNII
644VL95AO6

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name divalproex sodium (source: ndc)
Generic Name divalproex sodium (source: ndc)
Application Number ANDA078853 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7763-0)
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7763-1)
source: ndc

Packages (2)

50090-7763-0 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7763-0) 50090-7763-1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7763-1)

Ingredients (1)

divalproex sodium (250 mg/1)

Linked Drug Pages (1)

divalproex sodium ndc-match (0.9)

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"}