Hydroxyzine Hydrochloride 72789-0269-30

Package NDC

72789-0269-30

Manufacturer: Pd-Rx Pharmaceuticals, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 22, 2012
Listing Expires: December 31, 2026
Application: ANDA088619

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	50 mg/1

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

72789-0269-30Selected

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-269-30)