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divalproex sodium

NDC 29300-381, divalproex sodium, tablet, film coated, extended release, from Unichem Pharmaceuticals (USA), Inc..

Product NDC
29300-381
Status
Listed
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214643
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/29300-381 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM500 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
29300-381-0129300038101100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-01)
29300-381-0529300038105500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1d4129ae-0ce8-4a04-9f9d-c770508de8ed
  • NADAC price for package 29300038101

    GET /v1/drugs/nadac/29300038101
  • NADAC price for package 29300038105

    GET /v1/drugs/nadac/29300038105

Use it

Look up 29300-381 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/29300-381 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 29300-381. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.