Podocon 25 (Paddock Laboratories, LLC)
Welcome to the PulseAid listing for the Podocon 25 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: | Podophyllum resin |
SUBSTANCE NAME: | PODOPHYLLUM RESIN |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | TINCTURE |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 1990-09-01 |
END MARKETING DATE: | 0000-00-00 |
Podocon 25 HUMAN PRESCRIPTION DRUG Details:
Item Description | Podocon 25 from Paddock Laboratories, LLC |
LABELER NAME: | Paddock Laboratories, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1(mg/4mL) |
START MARKETING DATE: | 1990-09-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0574-0601_de96dc6e-e6d1-4383-9ce1-4d06bac08e00 |
PRODUCT NDC: | 0574-0601 |
APPLICATION NUMBER: | |
Other PODOPHYLLUM RESIN Pharmaceutical Manufacturers / Labelers: