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
- 59746-122_ead33f00-e158-464f-953f-ab5a9a391199
- Product NDC
- 59746-122
- Form
- TABLET
- Composition / generic term
- Meclizine Hydrochloride
- Labeler
- Jubilant Cadista Pharmacuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100604 / 20261031
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 (59746-122-06) · 59746-122-06
- 1000 TABLET in 1 BOTTLE (59746-122-10) · 59746-122-10
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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