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Chlorpromazine hydrochloride

NDC 16714-047 · Northstar Rx LLC

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

Packages

16714-047-01 — 100 TABLET, FILM COATED in 1 BOTTLE (16714-047-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0527-2965 — Chlorpromazine Hydrochloride, 0641-1397 — Chlorpromazine hydrochloride, 0641-1398 — Chlorpromazine hydrochloride, 0781-4027 — Chlorpromazine Hydrochloride, 0781-4028 — Chlorpromazine Hydrochloride, 0832-6017 — Chlorpromazine Hydrochloride, 0832-6018 — Chlorpromazine Hydrochloride, 0832-6019 — Chlorpromazine Hydrochloride, 0832-6020 — Chlorpromazine Hydrochloride, 0832-6021 — Chlorpromazine Hydrochloride, 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, +106 more

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