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Trifluridine
Trifluridine - 59762-0040-1 - (TRIFLURIDINE)
Drug Information of Trifluridine
| Product NDC: | 59762-0040 |
| Proprietary Name: | Trifluridine |
| Non Proprietary Name: | TRIFLURIDINE |
| Active Ingredient(s): | 1 g/100mL & nbsp; TRIFLURIDINE |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trifluridine
| Product NDC: | 59762-0040 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018299 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19800410 |
Package Information of Trifluridine
| Package NDC: | 59762-0040-1 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (59762-0040-1) > 7.5 mL in 1 BOTTLE, DROPPER |
NDC Information of Trifluridine
| NDC Code | 59762-0040-1 |
| Proprietary Name | Trifluridine |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (59762-0040-1) > 7.5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 59762-0040 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRIFLURIDINE |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19800410 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | TRIFLURIDINE |
| Strength Number | 1 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes | Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC] |
