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Levetiracetam

NDC 51672-4136, Levetiracetam, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4136
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078774
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4136 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVETIRACETAM100 mg/mL

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
51672-4136-0516724136003785 mL in 1 BOTTLE (51672-4136-0)
51672-4136-751672413607100 mL in 1 BOTTLE (51672-4136-7)
51672-4136-951672413609473 mL in 1 BOTTLE (51672-4136-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bf412e94-ca36-4da9-83d7-fb0f1323cf21

Use it

Look up 51672-4136 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4136 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4136. 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.