United States · FDA National Drug Code directory
MECLIZINE
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
- 71335-1215_dc78e0fc-fccc-45a2-a33b-2a2eeb5caab9
- Product NDC
- 71335-1215
- Form
- TABLET, CHEWABLE
- Composition / generic term
- Meclizine HCl 25mg
- Labeler
- Bryant Ranch Prepack
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start / end (source format)
- 20180201
- Source listing expiry
- 20261231
Source-listed ingredients
- MECLIZINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-0) · 71335-1215-0
- 30 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-1) · 71335-1215-1
- 20 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-2) · 71335-1215-2
- 25 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-3) · 71335-1215-3
- 40 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-4) · 71335-1215-4
- 60 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-5) · 71335-1215-5
- 90 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-6) · 71335-1215-6
- 8 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-7) · 71335-1215-7
- 14 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-8) · 71335-1215-8
- 10 TABLET, CHEWABLE in 1 BOTTLE (71335-1215-9) · 71335-1215-9
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 →