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: 68083-534_ffd998aa-4c6f-4463-b77c-9dc2e722b948
Product NDC: 68083-534
Form: INJECTION
Composition / generic term: Chlorpromazine hydrochloride
Labeler: Gland Pharma Limited
Marketing category: ANDA
Marketing start / end (source format): 20241004
Source listing expiry: 20261231

Source-listed ingredients

CHLORPROMAZINE HYDROCHLORIDE — 25 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

25 VIAL in 1 CARTON (68083-534-25) / 2 mL in 1 VIAL · 68083-534-25

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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