NDC 60687-664 – Hydroxyzine Hydrochloride

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

Human Prescription Drug

Product NDC60687-664

Product details

Brand name
Hydroxyzine Hydrochloride
Generic name
Hydroxyzine Hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA088617
Marketed since
October 13, 2022
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
60687-664-01100 BLISTER PACK in 1 CARTON (60687-664-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-664-11)Oct 13, 2022

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