NDC 70518-4141 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC70518-4141

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
July 16, 2024
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
70518-4141-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4141-0)Jul 16, 2024
70518-4141-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-1)Mar 26, 2025
70518-4141-290 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-2)Jul 15, 2025

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