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Divalproex Sodium

NDC 50268-260, Divalproex Sodium, tablet, extended release, from AvPAK.

Product NDC
50268-260
Status
Listed
Labeler
AvPAK
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203730
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50268-260 \
  -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
50268-260-135026802601330 BLISTER PACK in 1 BOX (50268-260-13) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-260-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e8cc336b-5191-7f8b-e053-2a95a90a6acb

  • NADAC price for package 50268026013

    GET /v1/drugs/nadac/50268026013

Use it

Look up 50268-260 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-260 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-260. 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.