Hydroxyzine Hydrochloride 68788-8707-03

Package NDC

68788-8707-03

Manufacturer: Preferred Pharmaceuticals Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 1, 2024
Listing Expires: December 31, 2027
Application: ANDA217652

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Active Ingredients

Ingredient	Strength
Hydroxyzine Hydrochloride	25 mg/1

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

68788-8707-03Selected

30 TABLET, FILM COATED in 1 BOTTLE (68788-8707-3)

Other packages for this product(2)

68788-8707-06

60 TABLET, FILM COATED in 1 BOTTLE (68788-8707-6)

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68788-8707-09

90 TABLET, FILM COATED in 1 BOTTLE (68788-8707-9)

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