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
0404-9965_38ebe239-ebab-4a1a-8b1e-aad0e36915ea
Product NDC
0404-9965
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Vancomycin Hydrochloride
Labeler
Henry Schein, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20220111
Source listing expiry
20261231

Source-listed ingredients

  • VANCOMYCIN HYDROCHLORIDE — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL in 1 BAG (0404-9965-99) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL · 0404-9965-99

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.

Browse United States records →