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vigabatrin

NDC 70771-1742, vigabatrin, powder, for solution, from Zydus Lifesciences Limited.

Product NDC
70771-1742
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214671
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1742 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VIGABATRIN500 mg/10mL

Pharmacologic classes

Anti-epileptic Agent [EPC]

Package NDCNDC-11Package
70771-1742-87077117420850 PACKET in 1 CARTON (70771-1742-8) / 10 mL in 1 PACKET (70771-1742-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cd5ebc7a-8d5b-46b4-ad9b-e4a25fa3e26c

Use it

Look up 70771-1742 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1742 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1742. 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.