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
- 0143-9161_d17179c5-783a-487a-ab74-fb8ad3eb9c34
- Product NDC
- 0143-9161
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- vancomycin hydrochloride
- Labeler
- HIKMA PHARMACEUTICALS USA INC.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20230202
- Source listing expiry
- 20261231
Source-listed ingredients
- VANCOMYCIN HYDROCHLORIDE — 513 mg/mg
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 PACKAGE (0143-9161-10) / 513 mg in 1 VIAL (0143-9161-01) · 0143-9161-10
- 25 VIAL in 1 PACKAGE (0143-9161-25) / 513 mg in 1 VIAL (0143-9161-01) · 0143-9161-25
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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