Actidose Aqua (Paddock Laboratories, LLC)
Welcome to the PulseAid listing for the Actidose Aqua drug offered from Paddock Laboratories, LLC. 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: | Paddock Laboratories, LLC |
NON-PROPRIETARY NAME: | activated charcoal |
SUBSTANCE NAME: | ACTIVATED CHARCOAL |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | SUSPENSION |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 1984-01-01 |
END MARKETING DATE: | 0000-00-00 |
Actidose Aqua HUMAN PRESCRIPTION DRUG Details:
Item Description | Actidose Aqua from Paddock Laboratories, LLC |
LABELER NAME: | Paddock Laboratories, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 208(mg/mL) |
START MARKETING DATE: | 1984-01-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0574-0121_a003785a-602c-4ac1-aa71-fa56b4329a6c |
PRODUCT NDC: | 0574-0121 |
APPLICATION NUMBER: | |
Other ACTIVATED CHARCOAL Pharmaceutical Manufacturers / Labelers: