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Trifluridine - 61314-044-75 - (trifluridine)

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Drug Information of Trifluridine

Product NDC: 61314-044
Proprietary Name: Trifluridine
Non Proprietary Name: trifluridine
Active Ingredient(s): 10    mg/mL & nbsp;   trifluridine
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Trifluridine

Product NDC: 61314-044
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074311
Marketing Category: ANDA
Start Marketing Date: 20010514

Package Information of Trifluridine

Package NDC: 61314-044-75
Package Description: 7.5 mL in 1 BOTTLE, PLASTIC (61314-044-75)

NDC Information of Trifluridine

NDC Code 61314-044-75
Proprietary Name Trifluridine
Package Description 7.5 mL in 1 BOTTLE, PLASTIC (61314-044-75)
Product NDC 61314-044
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name trifluridine
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20010514
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
Substance Name TRIFLURIDINE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC]

Complete Information of Trifluridine


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