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LATANOPROST - 52125-470-01 - (LATANOPROST)

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Drug Information of LATANOPROST

Product NDC: 52125-470
Proprietary Name: LATANOPROST
Non Proprietary Name: LATANOPROST
Active Ingredient(s): 50    ug/mL & nbsp;   LATANOPROST
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of LATANOPROST

Product NDC: 52125-470
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090887
Marketing Category: ANDA
Start Marketing Date: 20130612

Package Information of LATANOPROST

Package NDC: 52125-470-01
Package Description: 2.5 mL in 1 BOTTLE, DROPPER (52125-470-01)

NDC Information of LATANOPROST

NDC Code 52125-470-01
Proprietary Name LATANOPROST
Package Description 2.5 mL in 1 BOTTLE, DROPPER (52125-470-01)
Product NDC 52125-470
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LATANOPROST
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20130612
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LATANOPROST
Strength Number 50
Strength Unit ug/mL
Pharmaceutical Classes Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient]

Complete Information of LATANOPROST


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