NDC 71205-083 – Hydroxyzine Hydrochloride

Hydroxyzine Dihydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71205-083

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA088619
Marketed since
October 22, 2012
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
71205-083-1515 TABLET, FILM COATED in 1 BOTTLE (71205-083-15)Aug 1, 2018
71205-083-2020 TABLET, FILM COATED in 1 BOTTLE (71205-083-20)Aug 1, 2018
71205-083-3030 TABLET, FILM COATED in 1 BOTTLE (71205-083-30)Aug 1, 2018
71205-083-6060 TABLET, FILM COATED in 1 BOTTLE (71205-083-60)Aug 1, 2018
71205-083-9090 TABLET, FILM COATED in 1 BOTTLE (71205-083-90)Aug 1, 2018

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