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Divalproex Sodium

NDC 71610-032, Divalproex Sodium, tablet, delayed release, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-032
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078182
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-032 \
  -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
71610-032-537161000325360 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-53)
71610-032-607161000326090 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9cfdcb58-d6d7-43bb-b6e1-17172b143296

Use it

Look up 71610-032 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-032 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-032. 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.