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
- 72162-1775_25588ce8-86c6-4c3f-ad63-5271727c9124
- Product NDC
- 72162-1775
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- Vancomycin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190909
- Source listing expiry
- 20271231
Source-listed ingredients
- VANCOMYCIN HYDROCHLORIDE — 250 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 150 mL in 1 BOTTLE, PLASTIC (72162-1775-2) · 72162-1775-2
- 300 mL in 1 BOTTLE, PLASTIC (72162-1775-4) · 72162-1775-4
- 80 mL in 1 BOTTLE, PLASTIC (72162-1775-7) · 72162-1775-7
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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