NDC 71335-2340 – Hydroxyzine hydrochloride

Hydroxyzine Dihydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2340

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
71335-2340-130 TABLET in 1 BOTTLE (71335-2340-1)Jun 27, 2025
71335-2340-260 TABLET in 1 BOTTLE (71335-2340-2)Jun 27, 2025
71335-2340-320 TABLET in 1 BOTTLE (71335-2340-3)Jun 27, 2025
71335-2340-4100 TABLET in 1 BOTTLE (71335-2340-4)Jun 27, 2025
71335-2340-515 TABLET in 1 BOTTLE (71335-2340-5)Jun 27, 2025
71335-2340-690 TABLET in 1 BOTTLE (71335-2340-6)Jun 27, 2025
71335-2340-719 TABLET in 1 BOTTLE (71335-2340-7)Jun 27, 2025
71335-2340-810 TABLET in 1 BOTTLE (71335-2340-8)Jun 27, 2025

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