NDC 50742-339
Tafluprost 0.015 mg per 1 mL solution/ drops
On the label: Ingenus Pharmaceuticals, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kaysersberg Pharmaceuticals | Kaysersberg-Vignoble, France | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 17, 2024 · 4 inspections |
Product details
- Generic drug
- Tafluprost: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 0.015 mg per 1 mL
- Approval
- ANDA ANDA218002
- On the market since
- Dec 18, 2024
- Package NDCs
50742-339-0550742-339-30- Official label
- DailyMed (National Library of Medicine), updated Dec 4, 2024
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