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
55150-472_9aa42538-c84e-4886-8d3d-a7dfded5120f
Product NDC
55150-472
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Vancomycin hydrochloride
Labeler
Eugia US LLC
Marketing category
ANDA
Marketing start / end (source format)
20230804
Source listing expiry
20261231

Source-listed ingredients

  • VANCOMYCIN HYDROCHLORIDE — 1.5 g/30mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-472-10) / 30 mL in 1 VIAL, SINGLE-DOSE · 55150-472-10

Source and coverage

Open FDA National Drug Code directory

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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Vancomycin hydrochloride — United States | Molindra Medicines