NDC 10135-812 – Hydroxyzine Hydrochloride

Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC10135-812

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine hydrochloride
Labeler
Marlex Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207121
Marketed since
March 1, 2025
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
10135-812-01100 TABLET, FILM COATED in 1 BOTTLE (10135-812-01)Mar 1, 2025
10135-812-101000 TABLET, FILM COATED in 1 BOTTLE (10135-812-10)Mar 1, 2025

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