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
- 50268-522_47e73600-a8db-31d6-e063-6294a90a47f3
- Product NDC
- 50268-522
- Form
- TABLET
- Composition / generic term
- Meclizine
- Labeler
- AvPAK
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130808
- Source listing expiry
- 20271231
Source-listed ingredients
- MECLIZINE HYDROCHLORIDE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-522-15) / 1 TABLET in 1 BLISTER PACK (50268-522-11) · 50268-522-15
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 →