Dry Eye Test (Nomax Inc.)
Welcome to the PulseAid listing for the Dry Eye Test drug offered from Nomax Inc.. This Diagnostic Dye [EPC],Dyes [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: | Nomax Inc. |
| NON-PROPRIETARY NAME: | Fluorescein Sodium |
| SUBSTANCE NAME: | FLUORESCEIN SODIUM |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Diagnostic Dye [EPC],Dyes [MoA] |
| ROUTE: | OPHTHALMIC |
| DOSAGE FORM: | STRIP |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2013-12-05 |
| END MARKETING DATE: | 0000-00-00 |
Dry Eye Test HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dry Eye Test from Nomax Inc. |
| LABELER NAME: | Nomax Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.12(mg/1) |
| START MARKETING DATE: | 2013-12-05 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51801-008_08dd04c1-ca76-4b5d-ae29-1479238743b2 |
| PRODUCT NDC: | 51801-008 |
| APPLICATION NUMBER: | |
Other FLUORESCEIN SODIUM Pharmaceutical Manufacturers / Labelers:
