United States · FDA National Drug Code directory
Meclizine Hydrocloride
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
- 42708-102_459c95f7-ca90-7ded-e063-6394a90a0530
- Product NDC
- 42708-102
- Form
- TABLET
- Composition / generic term
- Meclizine Hydrocloride
- Labeler
- QPharma Inc
- 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
- 30 TABLET in 1 BOTTLE (42708-102-30) · 42708-102-30
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →