PODOFILOX (Paddock Laboratories, LLC)


Welcome to the PulseAid listing for the PODOFILOX drug offered from Paddock Laboratories, LLC. This Decreased Mitosis [PE] 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: PODOFILOX
SUBSTANCE NAME: PODOFILOX
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Decreased Mitosis [PE]
ROUTE: TOPICAL
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2002-01-29
END MARKETING DATE: 0000-00-00


PODOFILOX HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPODOFILOX from Paddock Laboratories, LLC
LABELER NAME: Paddock Laboratories, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 5(mg/mL)
START MARKETING DATE: 2002-01-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0574-0611_0374a375-639c-439d-914c-538b1e790c07
PRODUCT NDC: 0574-0611
APPLICATION NUMBER: ANDA075600

Other PODOFILOX Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Actavis Pharma, Inc.Condylox
Paddock Laboratories, LLCPODOFILOX
Physicians Total Care, Inc.Podofilox