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Latanoprost - 59762-0333-2 - (Latanoprost)

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Drug Information of Latanoprost

Product NDC: 59762-0333
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: 59762-0333
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020597
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19950320

Package Information of Latanoprost

Package NDC: 59762-0333-2
Package Description: 1 BOTTLE, DROPPER in 1 PACKAGE (59762-0333-2) > 2.5 mL in 1 BOTTLE, DROPPER

NDC Information of Latanoprost

NDC Code 59762-0333-2
Proprietary Name Latanoprost
Package Description 1 BOTTLE, DROPPER in 1 PACKAGE (59762-0333-2) > 2.5 mL in 1 BOTTLE, DROPPER
Product NDC 59762-0333
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Latanoprost
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19950320
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name LATANOPROST
Strength Number 50
Strength Unit ug/mL
Pharmaceutical Classes Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient]

Complete Information of Latanoprost


General Information