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: