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Divalproex Sodium

NDC 65862-403, Divalproex Sodium, tablet, delayed release, from Aurobindo Pharma Limited.

Product NDC
65862-403
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090554
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-403 \
  -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
65862-403-0165862040301100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-01)
65862-403-0565862040305500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-05)
65862-403-106586204031010 BLISTER PACK in 1 CARTON (65862-403-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
65862-403-22658620403222000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-22)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dbd47222-14f1-4588-a009-9b81b55ca60d

Use it

Look up 65862-403 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-403 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-403. 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.