Phocal Apf (U.S.I.A. Inc)
Welcome to the PulseAid listing for the Phocal Apf drug offered from U.S.I.A. Inc. This 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: | U.S.I.A. Inc |
| NON-PROPRIETARY NAME: | Sodium Fluoride, hydrofluoric acid |
| SUBSTANCE NAME: | SODIUM FLUORIDE; HYDROFLUORIC ACID |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | DISC |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2013-01-01 |
| END MARKETING DATE: | 0000-00-00 |
Phocal Apf HUMAN PRESCRIPTION DRUG Details:
| Item Description | Phocal Apf from U.S.I.A. Inc |
| LABELER NAME: | U.S.I.A. Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | .0466; .0094(mg/1; mg/1) |
| START MARKETING DATE: | 2013-01-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 55918-001_ac036ab4-3bae-41ac-a96a-ee269149ac19 |
| PRODUCT NDC: | 55918-001 |
| APPLICATION NUMBER: | |
Other SODIUM FLUORIDE; HYDROFLUORIC ACID Pharmaceutical Manufacturers / Labelers: