NDC 11534-206 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC11534-206

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine hydrochloride
Labeler
Sunrise Pharmaceutical, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207121
Marketed since
May 1, 2024
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
11534-206-01100 TABLET, FILM COATED in 1 BOTTLE (11534-206-01)May 1, 2024
11534-206-031000 TABLET, FILM COATED in 1 BOTTLE (11534-206-03)May 1, 2024
11534-206-04500 TABLET, FILM COATED in 1 BOTTLE (11534-206-04)Jan 10, 2025

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