Hydroxyzine Hydrochloride 00517-4201-25

Package NDC

00517-4201-25

Manufacturer: American Regent, Inc.
Dosage Form: Injection, Solution
Route: Intramuscular
Product Type: Human Prescription Drug
Marketing Start: September 30, 1990
Listing Expires: December 31, 2026
Application: ANDA087408

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	25 mg/mL

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

00517-4201-25Selected

25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4201-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0517-4201-01)