United States · FDA National Drug Code directory
Chlorpromazine
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
- 46708-739_1f9751ff-33da-44be-9c1f-9bbf88ac543b
- Product NDC
- 46708-739
- Form
- TABLET
- Composition / generic term
- Chlorpromazine
- Labeler
- Alembic Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230720
- Source listing expiry
- 20261231
Source-listed ingredients
- CHLORPROMAZINE HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 BLISTER PACK in 1 CARTON (46708-739-10) / 10 TABLET in 1 BLISTER PACK · 46708-739-10
- 100 TABLET in 1 BOTTLE (46708-739-31) · 46708-739-31
- 1000 TABLET in 1 BOTTLE (46708-739-91) · 46708-739-91
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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