United States · FDA National Drug Code directory
Vancomycin Hydrochloride
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
- 43538-805_18b06c9d-a2d4-4495-93c8-b6e42294eb2c
- Product NDC
- 43538-805
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Vancomycin hydrochloride
- Labeler
- Eurofarma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080630
- Source listing expiry
- 20271231
Source-listed ingredients
- VANCOMYCIN HYDROCHLORIDE — 500 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, GLASS in 1 CARTON (43538-805-10) / 10 mL in 1 VIAL, GLASS (43538-805-01) · 43538-805-10
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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