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
- 63323-314_d11a86ee-15b0-49cf-880a-f4b3b70e22cf
- Product NDC
- 63323-314
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Vancomycin Hydrochloride
- Labeler
- Fresenius Kabi, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170901
- Source listing expiry
- 20261231
Source-listed ingredients
- VANCOMYCIN HYDROCHLORIDE — 10 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (63323-314-68) / 100 mL in 1 BOTTLE · 63323-314-68
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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