NDC 23155-943 – Meclizine Hydrochloride

Meclizine Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-943

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205136
Marketed since
June 25, 2026
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
23155-943-01100 TABLET in 1 BOTTLE (23155-943-01)Jun 25, 2026
23155-943-101000 TABLET in 1 PACKAGE (23155-943-10)Jun 25, 2026

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