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Divalproex Sodium

NDC 71335-0008, Divalproex Sodium, tablet, delayed release, from Bryant Ranch Prepack.

Product NDC
71335-0008
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079163
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0008 \
  -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
71335-0008-17133500080130 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-1)
71335-0008-27133500080260 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-2)
71335-0008-37133500080390 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-3)
71335-0008-471335000804120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d67af03a-5261-4358-8787-2e729267ff7e

Use it

Look up 71335-0008 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0008 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0008. 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.