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: 70771-1697_d31d30de-9869-4ded-bb4d-c3b2ecbec440
Product NDC: 70771-1697
Form: TABLET
Composition / generic term: Prochlorperazine Maleate
Labeler: Zydus Lifesciences Limited
Marketing category: ANDA
Marketing start / end (source format): 20220810
Source listing expiry: 20261231

Source-listed ingredients

PROCHLORPERAZINE MALEATE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE (70771-1697-1) · 70771-1697-1

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.

Browse United States records →