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
- 71288-745_ef72e810-c31d-4c0a-8a7f-b1cfd8ac15ec
- Product NDC
- 71288-745
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Vecuronium Bromide
- Labeler
- Meitheal Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250701
- Source listing expiry
- 20261231
Source-listed ingredients
- VECURONIUM BROMIDE — 20 mg/20mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-USE in 1 CARTON (71288-745-21) / 20 mL in 1 VIAL, SINGLE-USE (71288-745-20) · 71288-745-21
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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