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Chlorpromazine Hydrochloride

NDC 59651-567 · Aurobindo Pharma Limited

Generic nameChlorpromazine Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)CHLORPROMAZINE HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classPhenothiazine [EPC], Phenothiazines [CS]
Marketing categoryANDA

Packages

59651-567-01 — 100 TABLET in 1 BOTTLE (59651-567-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50268-165 — CHLORPROMAZINE HYDROCHLORIDE, 50268-166 — CHLORPROMAZINE HYDROCHLORIDE, 51407-434 — Chlorpromazine Hydrochloride, 51407-435 — Chlorpromazine Hydrochloride, 51407-436 — Chlorpromazine Hydrochloride, 51407-437 — Chlorpromazine Hydrochloride, 51407-438 — Chlorpromazine Hydrochloride, 51662-1406 — CHLORPROMAZINE HCI, 55150-318 — CHLORPROMAZINE HYDROCHLORIDE, 55150-319 — CHLORPROMAZINE HYDROCHLORIDE, 59651-568 — Chlorpromazine Hydrochloride, 59651-569 — Chlorpromazine Hydrochloride, 59651-570 — Chlorpromazine Hydrochloride, 59651-571 — Chlorpromazine Hydrochloride, 60687-419 — CHLORPROMAZINE HYDROCHLORIDE, 60687-430 — CHLORPROMAZINE HYDROCHLORIDE, 60687-441 — CHLORPROMAZINE HYDROCHLORIDE, 60687-452 — CHLORPROMAZINE HYDROCHLORIDE, 60687-463 — CHLORPROMAZINE HYDROCHLORIDE, 60687-938 — Chlorpromazine Hydrochloride, +106 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.