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Divalproex Sodium

NDC 68788-4100, Divalproex Sodium, tablet, extended release, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4100
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090070
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4100 \
  -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
68788-4100-36878841000330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4100-3)
68788-4100-66878841000660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4100-6)
68788-4100-96878841000990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4100-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc9e4871-fb3d-4c59-81e5-2ab6e8be9b7c

Use it

Look up 68788-4100 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4100 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4100. 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.