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vecuronium bromide

NDC 47335-931, vecuronium bromide, injection, powder, lyophilized, for solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-931
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079001
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-931 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VECURONIUM BROMIDE1 mg/mL

Pharmacologic classes

Neuromuscular Nondepolarizing Blockade [PE]; Nondepolarizing Neuromuscular Blocker [EPC]

Package NDCNDC-11Package
47335-931-444733509314410 VIAL in 1 BOX (47335-931-44) / 10 mL in 1 VIAL (47335-931-40)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a14da3ee-a731-4282-be9d-407473517470

Use it

Look up 47335-931 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-931 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-931. 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.