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Divalproex sodium

NDC 68180-261, Divalproex sodium, tablet, extended release, from Lupin Pharmaceuticals, Inc..

Product NDC
68180-261
Status
Listed
Labeler
Lupin Pharmaceuticals, 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/68180-261 \
  -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
68180-261-0168180026101100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-01)
68180-261-0268180026102500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1f081c74-9f73-4ed9-9157-8d73d586a409

  • NADAC price for package 68180026101

    GET /v1/drugs/nadac/68180026101

  • NADAC price for package 68180026102

    GET /v1/drugs/nadac/68180026102

Use it

Look up 68180-261 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68180-261 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68180-261. 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.