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Divalproex Sodium

NDC 60760-798, Divalproex Sodium, tablet, delayed release, from St. Mary's Medical Park Pharmacy.

Product NDC
60760-798
Status
Listed
Labeler
St. Mary's Medical Park Pharmacy
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078597
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60760-798 \
  -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
60760-798-606076007986060 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-798-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/35a95333-9fc1-7a9f-e063-6294a90a9f30

Use it

Look up 60760-798 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60760-798 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60760-798. 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.