United States · FDA National Drug Code directory
DORZOLAMIDE HYDROCHLORIDE and TIMOLOL MALEATE
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
- 70069-051_81a3be92-0fdb-46c8-bc20-cd0947a2dbdf
- Product NDC
- 70069-051
- Form
- SOLUTION
- Composition / generic term
- DORZOLAMIDE HYDROCHLORIDE and TIMOLOL MALEATE
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190625
- Source listing expiry
- 20261231
Source-listed ingredients
- DORZOLAMIDE HYDROCHLORIDE — 20 mg/mL
- TIMOLOL MALEATE — 5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE · 70069-051-01
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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