VANIQA (Allergan, Inc.)


Welcome to the PulseAid listing for the VANIQA drug offered from Allergan, Inc.. This Antiprotozoal [EPC],Decarboxylase Inhibitor [EPC],Decarboxylase Inhibitors [MoA] 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: Allergan, Inc.
NON-PROPRIETARY NAME: eflornithine hydrochloride
SUBSTANCE NAME: EFLORNITHINE HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Antiprotozoal [EPC],Decarboxylase Inhibitor [EPC],Decarboxylase Inhibitors [MoA]
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-06-01
END MARKETING DATE: 0000-00-00


VANIQA HUMAN PRESCRIPTION DRUG Details:

Item DescriptionVANIQA from Allergan, Inc.
LABELER NAME: Allergan, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 139(mg/g)
START MARKETING DATE: 2013-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0023-4857_0cabbfd5-ec30-44a9-9f64-2532fa0cfe07
PRODUCT NDC: 0023-4857
APPLICATION NUMBER: NDA021145

Other EFLORNITHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allergan, Inc.VANIQA
Physicians Total Care, Inc.VANIQA