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
- 71205-647_bf1db485-1415-4229-b3e1-05a6f62ff7dd
- Product NDC
- 71205-647
- Form
- TABLET
- Composition / generic term
- Meclizine Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20200115
- Source listing expiry
- 20261231
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 (71205-647-10) · 71205-647-10
- 90 TABLET in 1 BOTTLE (71205-647-90) · 71205-647-90
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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