Hydroxyzine Hydrochloride 68071-4622-03

Package NDC

68071-4622-03

Manufacturer: Nucare Pharmaceuticals,inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 31, 2015
Listing Expires: December 31, 2026
Application: ANDA040602

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	25 mg/1

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

68071-4622-03Selected

30 TABLET, FILM COATED in 1 BOTTLE (68071-4622-3)