Folixapure (Shoreline Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Folixapure drug offered from Shoreline Pharmaceuticals, Inc.. This Vitamin D [Chemical/Ingredient],Vitamin D [EPC] 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: | Shoreline Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | Folic Acid, Vitamin D3 |
| SUBSTANCE NAME: | FOLIC ACID; VITAMIN D |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Vitamin D [Chemical/Ingredient],Vitamin D [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2016-05-13 |
| END MARKETING DATE: | 0000-00-00 |
Folixapure HUMAN PRESCRIPTION DRUG Details:
| Item Description | Folixapure from Shoreline Pharmaceuticals, Inc. |
| LABELER NAME: | Shoreline Pharmaceuticals, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1; 125(mg/1; ug/1) |
| START MARKETING DATE: | 2016-05-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 69621-090_ac948f39-89b1-49d3-9706-30df30a5782f |
| PRODUCT NDC: | 69621-090 |
| APPLICATION NUMBER: | |
Other FOLIC ACID; VITAMIN D Pharmaceutical Manufacturers / Labelers:
