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Chlorpromazine

NDC 46708-737 · Alembic Pharmaceuticals Limited

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

Packages

46708-737-10 — 100 BLISTER PACK in 1 CARTON (46708-737-10) / 10 TABLET in 1 BLISTER PACK

46708-737-31 — 100 TABLET in 1 BOTTLE (46708-737-31)

46708-737-91 — 1000 TABLET in 1 BOTTLE (46708-737-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16714-048 — Chlorpromazine hydrochloride, 16714-049 — Chlorpromazine hydrochloride, 16714-050 — Chlorpromazine hydrochloride, 16714-051 — Chlorpromazine hydrochloride, 31722-366 — chlorpromazine hydrochloride, 31722-367 — chlorpromazine hydrochloride, 43598-140 — CHLORPROMAZINE HCI, 43598-141 — CHLORPROMAZINE HCI, 46708-735 — Chlorpromazine, 46708-736 — Chlorpromazine, 46708-738 — Chlorpromazine, 46708-739 — Chlorpromazine, 50268-162 — CHLORPROMAZINE HYDROCHLORIDE, 50268-163 — CHLORPROMAZINE HYDROCHLORIDE, 50268-164 — CHLORPROMAZINE HYDROCHLORIDE, 50268-165 — CHLORPROMAZINE HYDROCHLORIDE, 50268-166 — CHLORPROMAZINE HYDROCHLORIDE, 51407-434 — Chlorpromazine Hydrochloride, 51407-435 — Chlorpromazine Hydrochloride, 51407-436 — 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.