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
- 0121-1032_1db451d1-f9ef-4e0a-8239-1c740369b64e
- Product NDC
- 0121-1032
- Form
- CAPSULE
- Composition / generic term
- VANCOMYCIN HYDROCHLORIDE
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260501
- Source listing expiry
- 20271231
Source-listed ingredients
- VANCOMYCIN HYDROCHLORIDE — 125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BLISTER PACK in 1 CARTON (0121-1032-20) / 10 CAPSULE in 1 BLISTER PACK · 0121-1032-20
- 50 CAPSULE in 1 BOTTLE (0121-1032-50) · 0121-1032-50
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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