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Thioridazine Hydrochloride

NDC 53489-148 · Sun Pharmaceutical Industries, Inc.

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

Packages

53489-148-01 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-148-01)

53489-148-10 — 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-148-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0378-0612 — thioridazine hydrochloride, 0378-0614 — thioridazine hydrochloride, 0378-0616 — thioridazine hydrochloride, 0378-0618 — thioridazine hydrochloride, 48433-095 — thioridazine hydrochloride, 48433-096 — thioridazine hydrochloride, 48433-097 — thioridazine hydrochloride, 48433-098 — thioridazine hydrochloride, 51079-565 — thioridazine hydrochloride, 51079-566 — thioridazine hydrochloride, 51079-567 — thioridazine hydrochloride, 51079-580 — thioridazine hydrochloride, 53489-149 — Thioridazine Hydrochloride, 53489-150 — Thioridazine Hydrochloride, 53489-500 — Thioridazine Hydrochloride, 62135-934 — Thioridazine Hydrochloride, 62135-936 — Thioridazine Hydrochloride, 62135-938 — Thioridazine Hydrochloride, 62135-939 — Thioridazine Hydrochloride

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