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divalproex sodium

NDC 68788-4193, divalproex sodium, tablet, film coated, extended release, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4193
Status
Listed
Labeler
Preferred Pharmaceuticals 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/68788-4193 \
  -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
68788-4193-36878841930330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4193-3)
68788-4193-66878841930660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4193-6)
68788-4193-96878841930990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4193-9)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2de86096-4ec7-47df-94db-9c7f6e5df424

Use it

Look up 68788-4193 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4193 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4193. 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.