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
- 71335-0503_50bf2686-9e05-4ae8-a8ee-761bea6f68e6
- Product NDC
- 71335-0503
- Form
- TABLET
- Composition / generic term
- Meclizine Hydrocloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100604 / 20261031
Source-listed ingredients
- MECLIZINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET in 1 BOTTLE (71335-0503-0) · 71335-0503-0
- 90 TABLET in 1 BOTTLE (71335-0503-1) · 71335-0503-1
- 30 TABLET in 1 BOTTLE (71335-0503-2) · 71335-0503-2
- 25 TABLET in 1 BOTTLE (71335-0503-3) · 71335-0503-3
- 20 TABLET in 1 BOTTLE (71335-0503-4) · 71335-0503-4
- 40 TABLET in 1 BOTTLE (71335-0503-5) · 71335-0503-5
- 60 TABLET in 1 BOTTLE (71335-0503-6) · 71335-0503-6
- 120 TABLET in 1 BOTTLE (71335-0503-7) · 71335-0503-7
- 10 TABLET in 1 BOTTLE (71335-0503-8) · 71335-0503-8
- 100 TABLET in 1 BOTTLE (71335-0503-9) · 71335-0503-9
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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