United States · FDA National Drug Code directory
Methazolamide
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
- 24208-023_41d745af-7d7b-dc08-e063-6394a90a2fbf
- Product NDC
- 24208-023
- Form
- TABLET
- Composition / generic term
- methazolamide
- Labeler
- Bausch & Lomb Incorporated
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201002
- Source listing expiry
- 20261231
Source-listed ingredients
- METHAZOLAMIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (24208-023-01) · 24208-023-01
- 100 TABLET in 1 BOTTLE (24208-023-10) · 24208-023-10
- 500 TABLET in 1 BOTTLE (24208-023-50) · 24208-023-50
- 90 TABLET in 1 BOTTLE (24208-023-90) · 24208-023-90
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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