NDC 70518-2066 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC70518-2066

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA088618
Marketed since
May 7, 2019
Listing expires
December 31, 2027
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
70518-2066-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-2066-0)May 7, 2019

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