Hydroxyzine Hydrochloride 67046-1311-03

Package NDC

67046-1311-03

Manufacturer: Coupler Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 12, 2026
Listing Expires: December 31, 2027
Application: ANDA217652

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	25 mg/1

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

67046-1311-03Selected

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1311-3)