Hydroxyzine Hydrochloride 10702-0011-10

Package NDC

10702-0011-10

Manufacturer: Kvk-Tech, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 24, 2012
Listing Expires: December 31, 2026
Application: ANDA040786

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	25 mg/1

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

10702-0011-10Selected

1000 TABLET, FILM COATED in 1 BOTTLE (10702-011-10)

Other packages for this product(2)

10702-0011-01

100 TABLET, FILM COATED in 1 BOTTLE (10702-011-01)

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10702-0011-50

500 TABLET, FILM COATED in 1 BOTTLE (10702-011-50)

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