NDC 24658-781 – Hydroxyzine Hydrochloride

Hydroxyzine Dihydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC24658-781

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040604
Marketed since
July 21, 2021
Listing expires
December 31, 2027
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
24658-781-05500 TABLET, FILM COATED in 1 BOTTLE (24658-781-05)Oct 24, 2024
24658-781-101000 TABLET, FILM COATED in 1 BOTTLE (24658-781-10)Jul 21, 2021

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