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Approved Drug Products containing 206185 listed in the FDA Orange Book. Original Data : FDA Website

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01 1SUN PHARM

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Brand Name : XELPROS

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Brand Name : XELPROS

Luxepack
Not Confirmed
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Sun Pharmaceutical Industries Limited

Dosage Form : EMULSION; OPHTHALMIC

Proprietary Name : XELPROS

Dosage Strength : 0.005%

Approval Date : 2018-09-12

Application Number : 206185

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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