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
- 0143-9355_e298d434-6e7e-4a46-9744-a098386a89d6
- Product NDC
- 0143-9355
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Vancomycin Hydrochloride
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181003
- Source listing expiry
- 20261231
Source-listed ingredients
- VANCOMYCIN — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (0143-9355-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9355-01) · 0143-9355-10
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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