XELPROS .05 mg/mL
latanoprost · SOLUTION/ DROPS · Sun Pharmaceutical Industries, Inc.
No Recall History
Plain English
XELPROS is a solution/ drops containing latanoprost at .05 mg/mL, taken ophthalmic. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- XELPROS
- Generic Name
- latanoprost
- NDC Code (Product)
47335-317- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- .05 mg/mL
- Dosage Form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC, TOPICAL
- Marketing Status
- Application #
- NDA206185
- Drug Class
- Prostaglandin Analog [EPC]
- Marketing Start
- 09/12/2018
Recall History
No Recall HistoryFrequently Asked Questions
What is XELPROS used for?
XELPROS contains latanoprost. It is a solution/ drops taken ophthalmic. Consult your doctor for specific uses.
Is XELPROS a controlled substance?
XELPROS is not classified as a controlled substance by the DEA.
What is the generic name for XELPROS?
The generic name for XELPROS is latanoprost. There are 11 other brand versions of latanoprost.
What is the NDC code for XELPROS .05 mg/mL?
The NDC (National Drug Code) for XELPROS .05 mg/mL is 47335-317, listed by Sun Pharmaceutical Industries, Inc..
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)