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
- 70710-1162_f084de6d-5e11-4c6e-8643-d0a4a48fc4da
- Product NDC
- 70710-1162
- Form
- TABLET
- Composition / generic term
- Meclizine Hydrochloride
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201029
- Source listing expiry
- 20261231
Source-listed ingredients
- MECLIZINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (70710-1162-0) · 70710-1162-0
- 100 TABLET in 1 BOTTLE (70710-1162-1) · 70710-1162-1
- 30 TABLET in 1 BOTTLE (70710-1162-3) · 70710-1162-3
- 10 BLISTER PACK in 1 CARTON (70710-1162-4) / 10 TABLET in 1 BLISTER PACK (70710-1162-2) · 70710-1162-4
- 90 TABLET in 1 BOTTLE (70710-1162-9) · 70710-1162-9
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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