NDC 70069-051
DORZOLAMIDE HYDROCHLORIDE and TIMOLOL MALEATE 5 mg per 1 mL / 20 mg per 1 mL solution
On the label: Somerset Therapeutics, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Somerset Therapeutics Private Limited | Bengaluru, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 21, 2025 · 10 inspections, 4 with FDA action |
Product details
- Generic drug
- Dorzolamide and Timolol: every company that makes it
- Form
- solution, ophthalmic
- Strength
- 5 mg per 1 mL / 20 mg per 1 mL
- Approval
- ANDA ANDA207523
- On the market since
- Jun 25, 2019
- Package NDCs
70069-051-01- Official label
- DailyMed (National Library of Medicine), updated Sep 18, 2024
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