Hydroxyzine Hydrochloride

NDC 0093-5062 · Teva Pharmaceuticals USA, Inc.

Generic nameHydroxyzine Hydrochloride

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)HYDROXYZINE DIHYDROCHLORIDE

Strength50 mg/1

Pharmacologic classAntihistamine [EPC], Histamine Receptor Antagonists [MoA]

Marketing categoryANDA

Packages

0093-5062-01 — 100 TABLET, FILM COATED in 1 BOTTLE (0093-5062-01)

0093-5062-05 — 500 TABLET, FILM COATED in 1 BOTTLE (0093-5062-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-5060 — Hydroxyzine Hydrochloride, 0093-5061 — Hydroxyzine Hydrochloride, 0121-1034 — hydroxyzine hydrochloride, 0404-9877 — Hydroxyzine Hydrochloride, 0404-9878 — Hydroxyzine, 0517-4201 — Hydroxyzine Hydrochloride, 0517-5601 — Hydroxyzine Hydrochloride, 0517-5602 — Hydroxyzine Hydrochloride, 0615-8082 — Hydroxyzine hydrochloride, 0615-8563 — Hydroxyzine hydrochloride, 0615-8564 — Hydroxyzine hydrochloride, 10135-810 — hydroxyzine hydrochloride, 10135-811 — hydroxyzine hydrochloride, 10135-812 — hydroxyzine hydrochloride, 10702-010 — hydroxyzine hydrochloride, 10702-011 — Hydroxyzine Hydrochloride, 10702-012 — Hydroxyzine Hydrochloride, 11534-204 — hydroxyzine hydrochloride, 11534-205 — hydroxyzine hydrochloride, 11534-206 — hydroxyzine hydrochloride, +151 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.