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
72162-1686_b972085a-db04-4f79-8542-c23317fea7df
Product NDC
72162-1686
Form
TABLET
Composition / generic term
Haloperidol
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20191125
Source listing expiry
20261231

Source-listed ingredients

  • HALOPERIDOL — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE (72162-1686-0) · 72162-1686-0
  • 100 TABLET in 1 BOTTLE (72162-1686-1) · 72162-1686-1

Source and coverage

Open FDA National Drug Code directory

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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