NDC 47335-317
Xelpros 0.05 mg per 1 mL solution/ drops
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Recalls
- Apr 22, 2024 · Class III · Sun Pharmaceutical Industries Inc
Failed Release Testing: Out of specification for particulate matter test.
Lots: Lot #: HAD3383A, Exp 8/31/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Latanoprost Acid: every company that makes it
- Form
- solution/ drops, ophthalmic; topical
- Strength
- 0.05 mg per 1 mL
- Approval
- NDA NDA206185
- On the market since
- Sep 12, 2018
- Package NDCs
47335-317-9047335-317-9247335-317-9447335-317-98- Official label
- DailyMed (National Library of Medicine), updated Dec 18, 2025
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