Hydroxyzine Hydrochloride 70954-0912-10

Package NDC

70954-0912-10

Manufacturer: Ani Pharmaceuticals, Inc.
Dosage Form: Solution
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 15, 2026
Listing Expires: December 31, 2026
Application: ANDA219648

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	10 mg/5mL

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

70954-0912-10Selected

473 mL in 1 BOTTLE (70954-912-10)