NDC 0093-5060 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC0093-5060

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA088617
Marketed since
February 19, 2013
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0093-5060-01100 TABLET, FILM COATED in 1 BOTTLE (0093-5060-01)Apr 8, 2013
0093-5060-05500 TABLET, FILM COATED in 1 BOTTLE (0093-5060-05)Feb 21, 2013

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