Alpha-Pro (Dental Technologies, Inc.)
Welcome to the PulseAid listing for the Alpha-Pro drug offered from Dental Technologies, 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: | Dental Technologies, Inc. |
NON-PROPRIETARY NAME: | Sodium Fluoride and Hydrofluoric Acid |
SUBSTANCE NAME: | SODIUM FLUORIDE; HYDROFLUORIC ACID |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | GEL |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2013-04-01 |
END MARKETING DATE: | 0000-00-00 |
Alpha-Pro HUMAN PRESCRIPTION DRUG Details:
Item Description | Alpha-Pro from Dental Technologies, Inc. |
LABELER NAME: | Dental Technologies, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 7.9; 4.4(mg/g; mg/g) |
START MARKETING DATE: | 2013-04-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 55346-0942_5b7fbec6-ecf3-49e1-97b1-0c2c71488fcf |
PRODUCT NDC: | 55346-0942 |
APPLICATION NUMBER: | |
Other SODIUM FLUORIDE; HYDROFLUORIC ACID Pharmaceutical Manufacturers / Labelers: