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VIGABATRIN

NDC 49884-358, vigabatrin, powder, for solution, from Par Health USA, LLC.

Product NDC
49884-358
Status
Listed
Labeler
Par Health USA, LLC
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208218
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49884-358 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VIGABATRIN50 mg/mL

Pharmacologic classes

Anti-epileptic Agent [EPC]

Package NDCNDC-11Package
49884-358-034988403580350 PACKET in 1 CARTON (49884-358-03) / 10 mL in 1 PACKET (49884-358-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e7cbc0a5-8c28-4451-9176-b608e228ba66

Use it

Look up 49884-358 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49884-358 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49884-358. 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.