NDC 72162-1333 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC72162-1333

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 (7)

Package NDCDescriptionSince
72162-1333-220 TABLET, FILM COATED in 1 BOTTLE (72162-1333-2)Apr 8, 2024
72162-1333-330 TABLET, FILM COATED in 1 BOTTLE (72162-1333-3)Apr 8, 2024
72162-1333-415 TABLET, FILM COATED in 1 BOTTLE (72162-1333-4)Apr 8, 2024
72162-1333-5500 TABLET, FILM COATED in 1 BOTTLE (72162-1333-5)Apr 8, 2024
72162-1333-660 TABLET, FILM COATED in 1 BOTTLE (72162-1333-6)Apr 8, 2024
72162-1333-810 TABLET, FILM COATED in 1 BOTTLE (72162-1333-8)Apr 8, 2024
72162-1333-990 TABLET, FILM COATED in 1 BOTTLE (72162-1333-9)Apr 8, 2024

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