NDC 0093-5061 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC0093-5061

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 · ANDA088618
Marketed since
October 9, 2012
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
0093-5061-01100 TABLET, FILM COATED in 1 BOTTLE (0093-5061-01)Oct 9, 2012
0093-5061-05500 TABLET, FILM COATED in 1 BOTTLE (0093-5061-05)Oct 10, 2012
0093-5061-101000 TABLET, FILM COATED in 1 BOTTLE (0093-5061-10)Oct 11, 2012

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