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
- 31722-210_e449bca2-14c8-ae21-e053-2a95a90a942b
- Product NDC
- 31722-210
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- VANCOMYCIN HYDROCHLORIDE
- Labeler
- Camber Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220706
- Source listing expiry
- 20261231
Source-listed ingredients
- VANCOMYCIN HYDROCHLORIDE — 500 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (31722-210-10) / 10 mL in 1 VIAL (31722-210-33) · 31722-210-10
- 25 VIAL in 1 CARTON (31722-210-32) / 10 mL in 1 VIAL (31722-210-33) · 31722-210-32
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 →