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Divalproex sodium

NDC 68788-8358, Divalproex sodium, tablet, extended release, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-8358
Status
Listed
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209286
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8358 \
  -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
68788-8358-36878883580330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-3)
68788-8358-66878883580660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-6)
68788-8358-96878883580990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/83a77f60-ed58-4fa0-a584-e6a0c767d19d

Use it

Look up 68788-8358 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8358 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8358. 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.