NDC 71335-1047 – Hydroxyzine Hydrochloride

Hydroxyzine Dihydrochloride 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1047

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040602
Marketed since
March 31, 2015
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-1047-130 TABLET, FILM COATED in 1 BOTTLE (71335-1047-1)Dec 27, 2018
71335-1047-260 TABLET, FILM COATED in 1 BOTTLE (71335-1047-2)Mar 13, 2020
71335-1047-320 TABLET, FILM COATED in 1 BOTTLE (71335-1047-3)Jun 19, 2019
71335-1047-4100 TABLET, FILM COATED in 1 BOTTLE (71335-1047-4)Apr 2, 2024
71335-1047-515 TABLET, FILM COATED in 1 BOTTLE (71335-1047-5)Feb 14, 2020
71335-1047-690 TABLET, FILM COATED in 1 BOTTLE (71335-1047-6)Oct 3, 2019
71335-1047-719 TABLET, FILM COATED in 1 BOTTLE (71335-1047-7)Apr 2, 2024
71335-1047-810 TABLET, FILM COATED in 1 BOTTLE (71335-1047-8)Feb 22, 2019

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