NDC 51655-080 – Hydroxyzine hydrochloride

Hydroxyzine Dihydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-080

Product details

Brand name
Hydroxyzine hydrochloride
Generic name
Hydroxyzine hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204279
Marketed since
December 10, 2020
Listing expires
December 31, 2027
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
51655-080-2020 TABLET in 1 BOTTLE, PLASTIC (51655-080-20)Apr 20, 2021
51655-080-2560 TABLET in 1 BOTTLE, PLASTIC (51655-080-25)Apr 15, 2022
51655-080-5230 TABLET in 1 BOTTLE, PLASTIC (51655-080-52)Dec 10, 2020
51655-080-5310 TABLET in 1 BOTTLE, PLASTIC (51655-080-53)Sep 13, 2023

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