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divalproex sodium

NDC 82804-233, divalproex sodium, tablet, delayed release, from Proficient Rx LP.

Product NDC
82804-233
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078853
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82804-233 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM250 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]; Mood Stabilizer [EPC]

Package NDCNDC-11Package
82804-233-308280402333030 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/15ffe3d8-d483-4c45-adc4-1cc8a5b68d19

Use it

Look up 82804-233 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-233 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-233. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.