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
82182-321_63e74b48-0ee2-40e8-a81f-008103768e17
Product NDC
82182-321
Form
SOLUTION/ DROPS
Composition / generic term
brimonidine tartrate
Labeler
Pacific Pharma, Inc.
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
20240102
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, DROPPER in 1 CARTON (82182-321-05) / 5 mL in 1 BOTTLE, DROPPER · 82182-321-05
  • 1 BOTTLE, DROPPER in 1 CARTON (82182-321-10) / 10 mL in 1 BOTTLE, DROPPER · 82182-321-10
  • 1 BOTTLE, DROPPER in 1 CARTON (82182-321-15) / 15 mL in 1 BOTTLE, DROPPER · 82182-321-15

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.

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Brimonidine tartrate — United States | Molindra Medicines