United States · FDA National Drug Code directory
Chlorpromazine hydrochloride
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
- 70710-1131_8a5df7d8-ad17-44d7-9c56-44fa2aaa0852
- Product NDC
- 70710-1131
- Form
- TABLET, FILM COATED
- Composition / generic term
- Chlorpromazine hydrochloride
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200127
- Source listing expiry
- 20261231
Source-listed ingredients
- CHLORPROMAZINE HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (70710-1131-1) · 70710-1131-1
- 10 BLISTER PACK in 1 CARTON (70710-1131-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1131-2) · 70710-1131-4
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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