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Levetiracetam

NDC 76494-531, Levetiracetam, tablet, film coated, from Prinston Pharmaceutical Inc..

Product NDC
76494-531
Status
Listed
Labeler
Prinston Pharmaceutical Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078106
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76494-531 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVETIRACETAM1000 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
76494-531-067649405310660 TABLET, FILM COATED in 1 BOTTLE (76494-531-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d818ef84-9b3e-434b-92d9-910cfa8af7da

Use it

Look up 76494-531 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76494-531 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76494-531. 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.