Hydroxyzine Hydrochloride 71656-0090-16

Package NDC

71656-0090-16

Manufacturer: Saptalis Pharmaceuticals, Llc.
Dosage Form: Solution
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 17, 2026
Listing Expires: December 31, 2027
Application: ANDA220271

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Active Ingredients

Ingredient	Strength
Hydroxyzine Hydrochloride	10 mg/5mL

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

71656-0090-16Selected

473 mL in 1 BOTTLE (71656-090-16)