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divalproex sodium

NDC 65841-639, divalproex sodium, capsule, coated pellets, from Zydus Lifesciences Limited.

Product NDC
65841-639
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
CAPSULE, COATED PELLETS
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078919
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65841-639 \
  -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
65841-639-0165841063901100 CAPSULE, COATED PELLETS in 1 BOTTLE (65841-639-01)
65841-639-10658410639101000 CAPSULE, COATED PELLETS in 1 BOTTLE (65841-639-10)
65841-639-306584106393010 BLISTER PACK in 1 CARTON (65841-639-30) / 10 CAPSULE, COATED PELLETS in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b0f33792-dd96-40cc-a28e-acdcdca2f4b8

Use it

Look up 65841-639 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-639 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-639. 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.