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
72162-2262_99b1f190-48d4-4f50-9ca3-8cda21fd37f0
Product NDC
72162-2262
Form
TABLET
Composition / generic term
Prochlorperazine maleate
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
19980301
Source listing expiry
20271231

Source-listed ingredients

  • PROCHLORPERAZINE MALEATE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (72162-2262-1) · 72162-2262-1

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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