United States · FDA National Drug Code directory
KETAMINE 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
- 0404-9882_1c76c787-2b29-4351-983c-a69a78636b52
- Product NDC
- 0404-9882
- Form
- INJECTION, SOLUTION, CONCENTRATE
- Composition / generic term
- ketamine hydrochloride
- Labeler
- Henry Schein, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220111
- Source listing expiry
- 20271231
Source-listed ingredients
- KETAMINE HYDROCHLORIDE — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 BAG (0404-9882-10) / 10 mL in 1 VIAL · 0404-9882-10
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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