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: 51655-096_4ab90401-073e-37f9-e063-6294a90a93f1
Product NDC: 51655-096
Form: TABLET
Composition / generic term: Prochlorperazine Maleate
Labeler: Northwind Health Company, LLC
Marketing category: ANDA
Marketing start / end (source format): 20140428
Source listing expiry: 20271231

Source-listed ingredients

PROCHLORPERAZINE MALEATE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

6 TABLET in 1 BOTTLE (51655-096-87) · 51655-096-87

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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