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Divalproex Sodium

NDC 70518-2674, Divalproex Sodium, tablet, delayed release, from REMEDYREPACK INC..

Product NDC
70518-2674
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/70518-2674 \
  -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
70518-2674-070518267400100 POUCH in 1 BOX (70518-2674-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2674-1)
70518-2674-27051826740230 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2674-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ed24bb3a-bba1-4b27-8733-96619793fc15

Use it

Look up 70518-2674 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2674 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2674. 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.