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CHLORPROMAZINE HYDROCHLORIDE

NDC 50268-162 · AvPAK

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

Packages

50268-162-15 — 50 BLISTER PACK in 1 BOX (50268-162-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-162-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 46708-737 — Chlorpromazine, 46708-738 — Chlorpromazine, 46708-739 — Chlorpromazine, 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, 51407-437 — Chlorpromazine Hydrochloride, 51407-438 — Chlorpromazine Hydrochloride, 51662-1406 — CHLORPROMAZINE HCI, +106 more

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