NDC 50090-6655 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC50090-6655

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
A-S Medication Solutions
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 (4)

Package NDCDescriptionSince
50090-6655-020 TABLET, FILM COATED in 1 BOTTLE (50090-6655-0)Aug 30, 2023
50090-6655-130 TABLET, FILM COATED in 1 BOTTLE (50090-6655-1)Aug 30, 2023
50090-6655-460 TABLET, FILM COATED in 1 BOTTLE (50090-6655-4)Aug 30, 2023
50090-6655-615 TABLET, FILM COATED in 1 BOTTLE (50090-6655-6)Aug 30, 2023

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