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Divalproex Sodium

NDC 68788-8609, Divalproex Sodium, tablet, delayed release, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8609
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078597
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8609 \
  -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
68788-8609-36878886090330 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-3)
68788-8609-66878886090660 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-6)
68788-8609-96878886090990 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d1d4d790-73d5-4a3b-a786-99f2c9812546

Use it

Look up 68788-8609 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8609 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8609. 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.