NDC 51655-589 – Hydroxyzine Hydrochloride

Hydroxyzine Dihydrochloride 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51655-589

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA088618
Marketed since
February 8, 2021
Listing expires
December 31, 2027
Pharmacologic class
Antihistamine

Active ingredients

Uses, dosage, side effects and warnings for Hydroxyzine Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
51655-589-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-25)Jan 10, 2024
51655-589-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-52)Jun 27, 2023
51655-589-5310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-53)Feb 8, 2021

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