NDC 70518-1730 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC70518-1730

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040787
Marketed since
December 13, 2018
Listing expires
December 31, 2027
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
70518-1730-530 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1730-5)Jun 18, 2025
70518-1730-690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1730-6)Jun 18, 2025
70518-1730-760 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1730-7)Oct 22, 2025

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