United States · FDA National Drug Code directory
PROMETHAZINE 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
- 39822-5550_0e860109-725f-1c28-e063-6394a90a50ef
- Product NDC
- 39822-5550
- Form
- INJECTION, SOLUTION
- Composition / generic term
- PROMETHAZINE HYDROCHLORIDE
- Labeler
- XGen Pharmaceuticals DJB, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150130
- Source listing expiry
- 20261231
Source-listed ingredients
- PROMETHAZINE HYDROCHLORIDE — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 AMPULE in 1 CARTON (39822-5550-6) / 1 mL in 1 AMPULE (39822-5550-5) · 39822-5550-6
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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