NDC 68788-8872 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC68788-8872

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217652
Marketed since
May 1, 2025
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
68788-8872-330 TABLET, FILM COATED in 1 BOTTLE (68788-8872-3)May 1, 2025

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