Hydroxyzine Hydrochloride 00093-5061-01

Package NDC

00093-5061-01

Manufacturer: Teva Pharmaceuticals Usa, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 9, 2012
Listing Expires: December 31, 2026
Application: ANDA088618

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	25 mg/1

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

00093-5061-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (0093-5061-01)

Other packages for this product(2)

00093-5061-05

500 TABLET, FILM COATED in 1 BOTTLE (0093-5061-05)

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00093-5061-10

1000 TABLET, FILM COATED in 1 BOTTLE (0093-5061-10)

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