Trifluridine (Greenstone LLC)
Welcome to the PulseAid listing for the Trifluridine drug offered from Greenstone LLC. This Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC],Nucleoside Metabolic Inhibitor [EPC],Nucleic Acid Synthesis Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Greenstone LLC |
| NON-PROPRIETARY NAME: | TRIFLURIDINE |
| SUBSTANCE NAME: | TRIFLURIDINE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC],Nucleoside Metabolic Inhibitor [EPC],Nucleic Acid Synthesis Inhibitors [MoA] |
| ROUTE: | OPHTHALMIC |
| DOSAGE FORM: | SOLUTION |
| MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
| START MARKETING DATE: | 1980-04-10 |
| END MARKETING DATE: | 2017-11-30 |
Trifluridine HUMAN PRESCRIPTION DRUG Details:
| Item Description | Trifluridine from Greenstone LLC |
| LABELER NAME: | Greenstone LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1(g/100mL) |
| START MARKETING DATE: | 1980-04-10 |
| END MARKETING DATE: | 2017-11-30 |
| PRODUCT ID: | 59762-0040_971e237b-ca18-481f-82ff-81de0935e54c |
| PRODUCT NDC: | 59762-0040 |
| APPLICATION NUMBER: | NDA018299 |
Other TRIFLURIDINE Pharmaceutical Manufacturers / Labelers:
