United States · FDA National Drug Code directory
Haloperidol
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
- 54838-501_898ee841-bdf7-4306-ac5c-282e522afd9f
- Product NDC
- 54838-501
- Form
- SOLUTION
- Composition / generic term
- Haloperidol
- Labeler
- Lannett Company, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19930928
- Source listing expiry
- 20261231
Source-listed ingredients
- HALOPERIDOL LACTATE — 2 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 15 mL in 1 BOTTLE, DROPPER (54838-501-15) · 54838-501-15
- 120 mL in 1 BOTTLE, DROPPER (54838-501-40) · 54838-501-40
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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