United States · FDA National Drug Code directory
Brinzolamide
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
- 0781-6014_dff324e7-139a-429e-989e-9d1ac7433d75
- Product NDC
- 0781-6014
- Form
- SUSPENSION/ DROPS
- Composition / generic term
- Brinzolamide
- Labeler
- Sandoz Inc
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20210308
- Source listing expiry
- 20261231
Source-listed ingredients
- BRINZOLAMIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (0781-6014-70) / 10 mL in 1 BOTTLE, PLASTIC · 0781-6014-70
- 1 BOTTLE, PLASTIC in 1 CARTON (0781-6014-85) / 15 mL in 1 BOTTLE, PLASTIC · 0781-6014-85
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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