United States · FDA National Drug Code directory

Brimonidine Tartrate

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
46708-749_ee26e0c9-a169-4842-ab0f-3c718bb14018
Product NDC
46708-749
Form
SOLUTION/ DROPS
Composition / generic term
Brimonidine Tartrate
Labeler
Alembic Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20230801
Source listing expiry
20261231

Source-listed ingredients

  • BRIMONIDINE TARTRATE — 1 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (46708-749-05) / 5 mL in 1 BOTTLE · 46708-749-05
  • 1 BOTTLE in 1 CARTON (46708-749-10) / 10 mL in 1 BOTTLE · 46708-749-10
  • 1 BOTTLE in 1 CARTON (46708-749-15) / 15 mL in 1 BOTTLE · 46708-749-15

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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