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, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

divalproex sodium 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7841
Product ID 50090-7841_21277d3e-ee56-48ad-a2b2-015dae50b6e9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214643
Listing Expiration 2027-12-31
Marketing Start 2022-02-25

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 500907841
Hyphenated Format 50090-7841

Supplemental Identifiers

RxCUI
1099569
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 ANDA214643 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-0)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-1)
source: ndc

Packages (2)

50090-7841-0 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-0) 50090-7841-1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-1)

Ingredients (1)

divalproex sodium (500 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": "21277d3e-ee56-48ad-a2b2-015dae50b6e9", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["e5fcf5b1-263e-43e0-9424-e613d5cca3fa"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-0)", "package_ndc": "50090-7841-0", "marketing_start_date": "20251229"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-1)", "package_ndc": "50090-7841-1", "marketing_start_date": "20251229"}], "brand_name": "divalproex sodium", "product_id": "50090-7841_21277d3e-ee56-48ad-a2b2-015dae50b6e9", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "50090-7841", "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": "500 mg/1"}], "application_number": "ANDA214643", "marketing_category": "ANDA", "marketing_start_date": "20220225", "listing_expiration_date": "20271231"}