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Divalproex Sodium

NDC 62756-797, Divalproex Sodium, tablet, delayed release, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-797
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/62756-797 \
  -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
62756-797-0862756079708100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-08)
62756-797-1362756079713500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-13)
62756-797-18627560797181000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18)
62756-797-836275607978330 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-83)
62756-797-8862756079788100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-88)

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 62756079713

    GET /v1/drugs/nadac/62756079713

  • NADAC price for package 62756079788

    GET /v1/drugs/nadac/62756079788

Use it

Look up 62756-797 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-797 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-797. 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.