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
- 72205-104_315ce03f-d9f8-4f3a-9e83-922747430c23
- Product NDC
- 72205-104
- Form
- TABLET, SUGAR COATED
- Composition / generic term
- Chlorpromazine Hydrochloride
- Labeler
- Novadoz Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220209
- Source listing expiry
- 20261231
Source-listed ingredients
- CHLORPROMAZINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, SUGAR COATED in 1 BOTTLE (72205-104-91) · 72205-104-91
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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