NDC 71205-332 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC71205-332

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040604
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
71205-332-1515 TABLET, FILM COATED in 1 BOTTLE (71205-332-15)Sep 1, 2019
71205-332-2020 TABLET, FILM COATED in 1 BOTTLE (71205-332-20)Sep 1, 2019
71205-332-3030 TABLET, FILM COATED in 1 BOTTLE (71205-332-30)Sep 1, 2019
71205-332-6060 TABLET, FILM COATED in 1 BOTTLE (71205-332-60)Sep 1, 2019
71205-332-9090 TABLET, FILM COATED in 1 BOTTLE (71205-332-90)Sep 1, 2019

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