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Divalproex sodium

NDC 0904-6615, Divalproex sodium, capsule, delayed release, from Major Pharmaceuticals.

Product NDC
0904-6615
Status
Listed
Labeler
Major Pharmaceuticals
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078979
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0904-6615 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM125 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]; Mood Stabilizer [EPC]

Package NDCNDC-11Package
0904-6615-6100904661561100 BLISTER PACK in 1 CARTON (0904-6615-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4a0fa934-ec8c-460e-86eb-11281728fe85

  • NADAC price for package 00904661561

    GET /v1/drugs/nadac/00904661561

Use it

Look up 0904-6615 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0904-6615 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0904-6615. 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.