United States · FDA National Drug Code directory

Meclizine HCl

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
57237-333_f603203c-84a4-4b41-a244-cff913e5c2e0
Product NDC
57237-333
Form
TABLET
Composition / generic term
MECLIZINE HYDROCHLORIDE
Labeler
Rising Pharma Holdings, Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20240722
Source listing expiry
20261231

Source-listed ingredients

  • MECLIZINE HYDROCHLORIDE — 12.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (57237-333-01) · 57237-333-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →