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Divalproex sodium

NDC 62332-821, Divalproex sodium, capsule, delayed release, from Alembic Pharmaceuticals Inc..

Product NDC
62332-821
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218793
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62332-821 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM125 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
62332-821-1062332082110100 BLISTER PACK in 1 CARTON (62332-821-10) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
62332-821-3162332082131100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-31)
62332-821-7162332082171500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-71)
62332-821-91623320821911000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fea19b14-d8ed-4954-bc54-b9240f78b3c3

Use it

Look up 62332-821 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-821 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-821. 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.