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 50090-1123
Product ID 50090-1123_063cd81a-e948-4ed6-aa2a-9cfeeacf0f57
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078597
Listing Expiration 2026-12-31
Marketing Start 2008-07-29

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 500901123
Hyphenated Format 50090-1123

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 ANDA078597 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-0)
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-1)
source: ndc

Packages (2)

50090-1123-0 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-0) 50090-1123-1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-1)

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": "063cd81a-e948-4ed6-aa2a-9cfeeacf0f57", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["c8f72850-92d5-4f64-b9f1-657f72bfa15a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-0)", "package_ndc": "50090-1123-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-1123-1)", "package_ndc": "50090-1123-1", "marketing_start_date": "20241024"}], "brand_name": "Divalproex Sodium", "product_id": "50090-1123_063cd81a-e948-4ed6-aa2a-9cfeeacf0f57", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "50090-1123", "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": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}