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Valproate Sodium

NDC 0143-9785, Valproate Sodium, injection, from Hikma Pharmaceuticals USA Inc..

Product NDC
0143-9785
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078523
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9785 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VALPROATE SODIUM500 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
0143-9785-100014397851010 VIAL, SINGLE-DOSE in 1 CARTON (0143-9785-10) / 5 mL in 1 VIAL, SINGLE-DOSE (0143-9785-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bcf57b31-4811-4104-82b3-46fb91a53ee0

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0143-9785

Use it

Look up 0143-9785 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9785 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0143-9785. 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.