NDC 63629-2432 – Meclizine Hydrochloride

Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-2432

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040659
Marketed since
June 4, 2010
Marketing end
October 31, 2026
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
63629-2432-11000 TABLET in 1 BOTTLE (63629-2432-1)Feb 25, 2021

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