NDC 70518-4170 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC70518-4170

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
hydroxyzine hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217652
Marketed since
August 28, 2024
Listing expires
December 31, 2027
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
70518-4170-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-0)Aug 28, 2024
70518-4170-190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-1)Apr 4, 2025
70518-4170-230 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-2)Jul 8, 2025
70518-4170-360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-3)Oct 24, 2025
70518-4170-490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-4)Dec 22, 2025
70518-4170-530 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-5)Apr 9, 2026

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