NDC 53746-442 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC53746-442

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201451
Marketed since
April 22, 2022
Listing expires
December 31, 2027
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
53746-442-01100 TABLET in 1 BOTTLE (53746-442-01)Apr 22, 2022
53746-442-101000 TABLET in 1 BOTTLE (53746-442-10)Apr 22, 2022

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