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Valproate Sodium

NDC 25021-797, Valproate Sodium, injection, solution, from Sagent Pharmaceuticals.

Product NDC
25021-797
Status
Listed
Labeler
Sagent Pharmaceuticals
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076295
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25021-797 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VALPROATE SODIUM100 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
25021-797-052502107970510 VIAL in 1 CARTON (25021-797-05) / 5 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8d5fc1c1-d3c0-497e-971b-6c4dba9a3fad

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=25021-797

Use it

Look up 25021-797 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25021-797 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25021-797. 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.