Hydroxyzine Hydrochloride 17856-0507-01

Package NDC

17856-0507-01

Manufacturer: Atlantic Biologicals Corp.
Dosage Form: Solution
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 21, 2013
Listing Expires: December 31, 2026
Application: ANDA201674

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	10 mg/5mL

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

17856-0507-01Selected

72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0507-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0507-2)