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:
