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Divalproex Sodium

NDC 68071-3553, Divalproex Sodium, tablet, delayed release, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-3553
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
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/68071-3553 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM250 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68071-3553-66807135530660 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3553-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0bef10ed-e4b5-95ae-e063-6294a90a86eb

Use it

Look up 68071-3553 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3553 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3553. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.