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Chlorpromazine hydrochloride

NDC 70771-1508 · Zydus Lifesciences Limited

Generic nameChlorpromazine hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CHLORPROMAZINE HYDROCHLORIDE
Strength50 mg/1
Pharmacologic classPhenothiazine [EPC], Phenothiazines [CS]
Marketing categoryANDA

Packages

70771-1508-1 — 100 TABLET, FILM COATED in 1 BOTTLE (70771-1508-1)

70771-1508-4 — 10 BLISTER PACK in 1 CARTON (70771-1508-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1508-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4295 — Chlorpromazine Hydrochloride, 70710-1129 — Chlorpromazine hydrochloride, 70710-1130 — Chlorpromazine hydrochloride, 70710-1131 — Chlorpromazine hydrochloride, 70710-1132 — Chlorpromazine hydrochloride, 70710-1133 — Chlorpromazine hydrochloride, 70710-1849 — Chlorpromazine Hydrochloride, 70710-1850 — Chlorpromazine Hydrochloride, 70771-1506 — Chlorpromazine hydrochloride, 70771-1507 — Chlorpromazine hydrochloride, 70771-1509 — Chlorpromazine hydrochloride, 70771-1510 — Chlorpromazine hydrochloride, 70771-1778 — Chlorpromazine Hydrochloride, 70771-1779 — Chlorpromazine Hydrochloride, 71656-101 — Chlorpromazine Hydrochloride, 71656-102 — Chlorpromazine Hydrochloride, 72205-104 — Chlorpromazine Hydrochloride, 72205-105 — Chlorpromazine Hydrochloride, 72205-106 — Chlorpromazine Hydrochloride, 72205-107 — 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.