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Divalproex Sodium

NDC 70518-3431, Divalproex Sodium, tablet, delayed release, from REMEDYREPACK INC..

Product NDC
70518-3431
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078597
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3431 \
  -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
70518-3431-07051834310060 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3431-0)
70518-3431-270518343102100 POUCH in 1 BOX (70518-3431-2) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3431-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bb94bbb1-07c1-49be-8c2c-f5635c65366d

Use it

Look up 70518-3431 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3431 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3431. 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.