NDC 71335-3036 – Hydroxyzine Hydrochloride

Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-3036

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA087871
Marketed since
October 7, 2021
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
71335-3036-11000 TABLET, FILM COATED in 1 BOTTLE (71335-3036-1)Dec 3, 2025

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