Hydroxyzine Hydrochloride 68788-8872-03

Package NDC

68788-8872-03

Manufacturer: Preferred Pharmaceuticals Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 1, 2025
Listing Expires: December 31, 2026
Application: ANDA217652

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	10 mg/1

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

68788-8872-03Selected

30 TABLET, FILM COATED in 1 BOTTLE (68788-8872-3)