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
- 59746-115_15ccaf96-5c2f-45cb-992c-99f5458da55b
- Product NDC
- 59746-115
- Form
- TABLET
- Composition / generic term
- Prochlorperazine maleate
- Labeler
- Jubilant Cadista Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19980301
- Source listing expiry
- 20261231
Source-listed ingredients
- PROCHLORPERAZINE MALEATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (59746-115-06) · 59746-115-06
- 1000 TABLET in 1 BOTTLE (59746-115-10) · 59746-115-10
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 →