United States · FDA National Drug Code directory

Meclizine Hydrochloride

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: 80425-0494_2d31baa5-5e96-61fa-e063-6394a90a7413
Product NDC: 80425-0494
Form: TABLET
Composition / generic term: Meclizine Hydrochloride
Labeler: Advanced Rx of Tennessee, LLC
Marketing category: NDA AUTHORIZED GENERIC
Marketing start / end (source format): 20250202
Source listing expiry: 20261231

Source-listed ingredients

MECLIZINE HYDROCHLORIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE (80425-0494-1) · 80425-0494-1
60 TABLET in 1 BOTTLE (80425-0494-2) · 80425-0494-2
90 TABLET in 1 BOTTLE (80425-0494-3) · 80425-0494-3

Source and coverage

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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.

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