United States · FDA National Drug Code directory
Brimonidine
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
- 0781-7177_185d0bdc-55b3-4d7d-9fc2-225345dfe28b
- Product NDC
- 0781-7177
- Form
- SOLUTION/ DROPS
- Composition / generic term
- brimonidine tartrate
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240304
- Source listing expiry
- 20271231
Source-listed ingredients
- BRIMONIDINE TARTRATE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DROPPER in 1 CARTON (0781-7177-70) / 10 mL in 1 BOTTLE, DROPPER · 0781-7177-70
- 1 BOTTLE, DROPPER in 1 CARTON (0781-7177-75) / 5 mL in 1 BOTTLE, DROPPER · 0781-7177-75
- 1 BOTTLE, DROPPER in 1 CARTON (0781-7177-85) / 15 mL in 1 BOTTLE, DROPPER · 0781-7177-85
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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