United States · FDA National Drug Code directory
vecuronium bromide
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 47335-931_575c52a5-c108-0a7e-e063-6294a90a5e38
- Product NDC
- 47335-931
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- vecuronium bromide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141215 / 20270331
Source-listed ingredients
- VECURONIUM BROMIDE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 BOX (47335-931-44) / 10 mL in 1 VIAL (47335-931-40) · 47335-931-44
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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