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Latanoprost - 60505-0565-0 - (Latanoprost)

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Drug Information of Latanoprost

Product NDC: 60505-0565
Proprietary Name: Latanoprost
Non Proprietary Name: Latanoprost
Active Ingredient(s): 50    ug/mL & nbsp;   Latanoprost
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Latanoprost

Product NDC: 60505-0565
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077697
Marketing Category: ANDA
Start Marketing Date: 20110322

Package Information of Latanoprost

Package NDC: 60505-0565-0
Package Description: 3 BOTTLE, DROPPER in 1 CARTON (60505-0565-0) > 2.5 mL in 1 BOTTLE, DROPPER

NDC Information of Latanoprost

NDC Code 60505-0565-0
Proprietary Name Latanoprost
Package Description 3 BOTTLE, DROPPER in 1 CARTON (60505-0565-0) > 2.5 mL in 1 BOTTLE, DROPPER
Product NDC 60505-0565
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Latanoprost
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20110322
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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