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Divalproex sodium

NDC 72162-2516, Divalproex sodium, tablet, film coated, extended release, from Bryant Ranch Prepack.

Product NDC
72162-2516
Status
Listed
Labeler
Bryant Ranch Prepack
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/72162-2516 \
  -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
72162-2516-172162251601100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-1)
72162-2516-572162251605500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0669ac77-10df-48af-bc42-55e768b69e4f

Use it

Look up 72162-2516 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2516 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-2516. 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.