NDC 71610-735 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC71610-735

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040602
Marketed since
March 31, 2015
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71610-735-3030 TABLET, FILM COATED in 1 BOTTLE (71610-735-30)Sep 14, 2023
71610-735-5360 TABLET, FILM COATED in 1 BOTTLE (71610-735-53)Sep 14, 2023
71610-735-6090 TABLET, FILM COATED in 1 BOTTLE (71610-735-60)Sep 14, 2023
71610-735-70120 TABLET, FILM COATED in 1 BOTTLE (71610-735-70)Sep 14, 2023
71610-735-80180 TABLET, FILM COATED in 1 BOTTLE (71610-735-80)Sep 14, 2023

Other Hydroxyzine Hydrochloride products