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Divalproex sodium

NDC 16714-485, Divalproex sodium, tablet, film coated, extended release, from NorthStar Rx LLC.

Product NDC
16714-485
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202419
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-485 \
  -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
16714-485-0116714048501100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-485-01)
16714-485-0216714048502500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-485-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aab6b411-11e9-4a16-afb6-d471ba4756e9

  • NADAC price for package 16714048501

    GET /v1/drugs/nadac/16714048501

  • NADAC price for package 16714048502

    GET /v1/drugs/nadac/16714048502

Use it

Look up 16714-485 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-485 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-485. 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.