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
63323-474_f3409439-088d-49ec-9e10-c6c3b1a07eef
Product NDC
63323-474
Form
INJECTION, SOLUTION
Composition / generic term
HALOPERIDOL LACTATE
Labeler
Fresenius Kabi USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20001020
Source listing expiry
20261231

Source-listed ingredients

  • HALOPERIDOL LACTATE — 5 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 25 VIAL in 1 TRAY (63323-474-01) / 1 mL in 1 VIAL (63323-474-00) · 63323-474-01
  • 1 VIAL, MULTI-DOSE in 1 BOX (63323-474-10) / 10 mL in 1 VIAL, MULTI-DOSE · 63323-474-10

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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