Oxytrol For Women (Actavis Pharma, Inc.)


Welcome to the PulseAid listing for the Oxytrol For Women drug offered from Actavis Pharma, Inc.. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: Actavis Pharma, Inc.
NON-PROPRIETARY NAME: oxybutynin
SUBSTANCE NAME: OXYBUTYNIN
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TRANSDERMAL
DOSAGE FORM: PATCH
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2016-01-01
END MARKETING DATE: 0000-00-00


Oxytrol For Women HUMAN OTC DRUG Details:

Item DescriptionOxytrol For Women from Actavis Pharma, Inc.
LABELER NAME: Actavis Pharma, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3.9(mg/d)
START MARKETING DATE: 2016-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 52544-166_9b87a67d-bbce-4cae-b365-b36d96b0cc6b
PRODUCT NDC: 52544-166
APPLICATION NUMBER: NDA202211

Other OXYBUTYNIN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Actavis Pharma, Inc.Gelnique
Allergan, Inc.OXYTROL