Hydroxyzine Hydrochloride 00121-1034-16

Package NDC

00121-1034-16

Manufacturer: Pai Holdings, Llc Dba Pai Pharma
Dosage Form: Solution
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: April 10, 2002
Listing Expires: December 31, 2026
Application: ANDA040391

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	10 mg/5mL

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

00121-1034-16Selected

473 mL in 1 BOTTLE (0121-1034-16)