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Divalproex sodium

NDC 65862-594, Divalproex sodium, tablet, film coated, extended release, from Aurobindo Pharma Limited.

Product NDC
65862-594
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202419
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-594 \
  -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
65862-594-0165862059401100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-01)
65862-594-0565862059405500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-05)
65862-594-106586205941010 BLISTER PACK in 1 CARTON (65862-594-10) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
65862-594-606586205946060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-60)
65862-594-99658620594991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6240cee7-6aa8-425c-ba46-f889a640f0fa

  • NADAC price for package 65862059401

    GET /v1/drugs/nadac/65862059401

  • NADAC price for package 65862059499

    GET /v1/drugs/nadac/65862059499

Use it

Look up 65862-594 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-594 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-594. 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.