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Latanoprost - 61314-547-03 - (Latanoprost)

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Drug Information of Latanoprost

Product NDC: 61314-547
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: 61314-547
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091449
Marketing Category: ANDA
Start Marketing Date: 20110107

Package Information of Latanoprost

Package NDC: 61314-547-03
Package Description: 2.5 mL in 1 BOTTLE (61314-547-03)

NDC Information of Latanoprost

NDC Code 61314-547-03
Proprietary Name Latanoprost
Package Description 2.5 mL in 1 BOTTLE (61314-547-03)
Product NDC 61314-547
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Latanoprost
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20110107
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
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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