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Divalproex Sodium

NDC 62756-798, Divalproex Sodium, tablet, delayed release, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-798
Status
Listed
Labeler
Sun Pharmaceutical Industries, 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/62756-798 \
  -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
62756-798-0862756079808100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-08)
62756-798-1362756079813500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-13)
62756-798-18627560798181000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-18)
62756-798-836275607988330 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-83)
62756-798-8862756079888100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/64797788-fdcb-4d12-a1a4-743ad71bd17b

  • NADAC price for package 62756079813

    GET /v1/drugs/nadac/62756079813

  • NADAC price for package 62756079888

    GET /v1/drugs/nadac/62756079888

Use it

Look up 62756-798 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-798 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-798. 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.