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