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Valproate Sodium

NDC 63323-494, VALPROATE SODIUM, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
63323-494
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076539
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63323-494 \
  -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
63323-494-056332304940510 VIAL, SINGLE-DOSE in 1 TRAY (63323-494-05) / 5 mL in 1 VIAL, SINGLE-DOSE (63323-494-01)
63323-494-166332304941610 VIAL, SINGLE-DOSE in 1 TRAY (63323-494-16) / 5 mL in 1 VIAL, SINGLE-DOSE (63323-494-41)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels?ndc=63323-494
  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=63323-494

Use it

Look up 63323-494 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63323-494 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63323-494. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.