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: 68788-8633_9628e3fe-56fd-4fcc-a540-b8000b7232ba
Product NDC: 68788-8633
Form: TABLET
Composition / generic term: Meclizine Hydrochloride
Labeler: Preferred Pharmaceuticals Inc.
Marketing category: NDA AUTHORIZED GENERIC
Marketing start / end (source format): 20240416
Source listing expiry: 20271231

Source-listed ingredients

MECLIZINE HYDROCHLORIDE — 12.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

10 TABLET in 1 BOTTLE (68788-8633-1) · 68788-8633-1
30 TABLET in 1 BOTTLE (68788-8633-3) · 68788-8633-3

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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