NDC 72162-1332 – Hydroxyzine Hydrochloride

Hydroxyzine Dihydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72162-1332

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040600
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 (2)

Package NDCDescriptionSince
72162-1332-330 TABLET, FILM COATED in 1 BOTTLE (72162-1332-3)Apr 8, 2024
72162-1332-990 TABLET, FILM COATED in 1 BOTTLE (72162-1332-9)Apr 8, 2024

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