NDC 43063-518 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC43063-518

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040787
Marketed since
July 24, 2012
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
43063-518-066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-06)Jul 24, 2012
43063-518-1212 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-12)Jul 24, 2012
43063-518-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-20)Jul 24, 2012
43063-518-2828 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-28)Jul 24, 2012
43063-518-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-30)Jul 24, 2012
43063-518-4040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-40)Jul 24, 2012
43063-518-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-60)Dec 18, 2019
43063-518-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-90)Jul 24, 2012

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