NDC 71335-0935 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC71335-0935

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA088618
Marketed since
October 9, 2012
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
71335-0935-130 TABLET, FILM COATED in 1 BOTTLE (71335-0935-1)Aug 28, 2018
71335-0935-260 TABLET, FILM COATED in 1 BOTTLE (71335-0935-2)Aug 28, 2018
71335-0935-320 TABLET, FILM COATED in 1 BOTTLE (71335-0935-3)Aug 28, 2018
71335-0935-4100 TABLET, FILM COATED in 1 BOTTLE (71335-0935-4)Aug 28, 2018
71335-0935-515 TABLET, FILM COATED in 1 BOTTLE (71335-0935-5)Aug 28, 2018
71335-0935-690 TABLET, FILM COATED in 1 BOTTLE (71335-0935-6)Aug 28, 2018
71335-0935-719 TABLET, FILM COATED in 1 BOTTLE (71335-0935-7)Aug 28, 2018
71335-0935-810 TABLET, FILM COATED in 1 BOTTLE (71335-0935-8)Aug 28, 2018

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