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Divalproex sodium

NDC 70518-3477, Divalproex sodium, tablet, extended release, from REMEDYREPACK INC..

Product NDC
70518-3477
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209286
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3477 \
  -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
70518-3477-07051834770030 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3477-0)
70518-3477-17051834770130 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3477-1)
70518-3477-370518347703100 POUCH in 1 BOX (70518-3477-3) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-4)
70518-3477-570518347705100 POUCH in 1 BOX (70518-3477-5) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6af40b06-0a92-454c-9277-80e89de27231

Use it

Look up 70518-3477 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3477 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3477. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.