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 DescriptionPodocon 25 from Paddock Laboratories, LLC
LABELER NAME: Paddock Laboratories, LLC
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Paddock Laboratories, LLCPodocon 25
Washington Homeopathic ProductsPodophyllinum