LATANOPROST 50 ug/mL
LATANOPROST · SOLUTION/ DROPS · Somerset Therapeutics, LLC
No Recall History
Plain English
LATANOPROST is a solution/ drops containing latanoprost at 50 ug/mL, taken ophthalmic. Manufactured by Somerset Therapeutics, LLC.
Key Facts
- Brand Name
- LATANOPROST
- Generic Name
- LATANOPROST
- NDC Code (Product)
70069-421- Manufacturer
- Somerset Therapeutics, LLC
- Strength
- 50 ug/mL
- Dosage Form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Marketing Status
- Application #
- ANDA201786
- Drug Class
- Prostaglandin Analog [EPC]
- Marketing Start
- 12/03/2019
Recall History
No Recall HistoryFrequently Asked Questions
What is LATANOPROST used for?
LATANOPROST contains LATANOPROST. It is a solution/ drops taken ophthalmic. Consult your doctor for specific uses.
Is LATANOPROST a controlled substance?
LATANOPROST is not classified as a controlled substance by the DEA.
What is the generic name for LATANOPROST?
The generic name for LATANOPROST is LATANOPROST. There are 10 other brand versions of LATANOPROST.
What is the NDC code for LATANOPROST 50 ug/mL?
The NDC (National Drug Code) for LATANOPROST 50 ug/mL is 70069-421, listed by Somerset Therapeutics, LLC.
Other LATANOPROST Dosages
Other Latanoprost Brands
See all →- Latanoprost50 ug/mL50090-7062
- Latanoprost50 ug/mL61314-547
- Latanoprostene Bunod Ophthalmic Solution, 0.024%.24 mg/mL68083-563
- IYUZEH50 ug/mL82584-003
- Latanoprost50 ug/mL25021-001
- Latanoprost50 ug/mL50090-1920
- Latanoprost50 ug/mL65862-872
- Latanoprost50 ug/mL71205-154
- Latanoprost50 ug/mL42571-499
- XELPROS.05 mg/mL47335-317
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)