NDC 71335-0268 – Hydroxyzine hydrochloride

Hydroxyzine Dihydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0268

Product details

Brand name
Hydroxyzine hydrochloride
Generic name
Hydroxyzine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204279
Marketed since
August 20, 2014
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-0268-130 TABLET in 1 BOTTLE (71335-0268-1)Apr 5, 2018
71335-0268-2100 TABLET in 1 BOTTLE (71335-0268-2)Feb 2, 2022
71335-0268-320 TABLET in 1 BOTTLE (71335-0268-3)Jun 25, 2021
71335-0268-490 TABLET in 1 BOTTLE (71335-0268-4)May 4, 2018
71335-0268-515 TABLET in 1 BOTTLE (71335-0268-5)Feb 2, 2022
71335-0268-660 TABLET in 1 BOTTLE (71335-0268-6)Feb 2, 2022
71335-0268-7120 TABLET in 1 BOTTLE (71335-0268-7)Feb 2, 2022
71335-0268-810 TABLET in 1 BOTTLE (71335-0268-8)Feb 20, 2018

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