Hydroxyzine Hydrochloride 16571-0115-01

Package NDC

16571-0115-01

Manufacturer: Rising Pharma Holdings, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 22, 2023
Listing Expires: December 31, 2026
Application: ANDA217652

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Active Ingredients

Ingredient	Strength
Hydroxyzine Dihydrochloride	50 mg/1

Drug Class

Antihistamine [EPC]Histamine Receptor Antagonists [MoA]

Selected Package

16571-0115-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (16571-115-01)

Other packages for this product(2)

16571-0115-10

1000 TABLET, FILM COATED in 1 BOTTLE (16571-115-10)

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16571-0115-50

500 TABLET, FILM COATED in 1 BOTTLE (16571-115-50)

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