Trifluridine (Hi-Tech Pharmacal Co., Inc.)
Welcome to the PulseAid listing for the Trifluridine drug offered from Hi-Tech Pharmacal Co., Inc.. 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: | Hi-Tech Pharmacal Co., Inc. |
| 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/ DROPS |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2017-07-28 |
| END MARKETING DATE: | 0000-00-00 |
Trifluridine HUMAN PRESCRIPTION DRUG Details:
| Item Description | Trifluridine from Hi-Tech Pharmacal Co., Inc. |
| LABELER NAME: | Hi-Tech Pharmacal Co., Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 2017-07-28 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50383-955_e9f0104c-2506-4ddb-bae2-342c73a24ee3 |
| PRODUCT NDC: | 50383-955 |
| APPLICATION NUMBER: | ANDA205438 |
Other TRIFLURIDINE Pharmaceutical Manufacturers / Labelers:
