United States · FDA National Drug Code directory

PROCHLORPERAZINE MALEATE

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
66267-271_1fa6a518-e71d-2232-e063-6294a90a73e4
Product NDC
66267-271
Form
TABLET
Composition / generic term
Prochlorperazine Maleate
Labeler
NuCare Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
19980301
Source listing expiry
20261231

Source-listed ingredients

  • PROCHLORPERAZINE MALEATE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (66267-271-30) · 66267-271-30

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.

Browse United States records →