Duloxetine (Camber Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the Duloxetine drug offered from Camber Pharmaceuticals, Inc.. This Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake 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: Camber Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: Duloxetine
SUBSTANCE NAME: DULOXETINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
ROUTE: ORAL
DOSAGE FORM: CAPSULE, DELAYED RELEASE
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2016-08-11
END MARKETING DATE: 0000-00-00


Duloxetine HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDuloxetine from Camber Pharmaceuticals, Inc.
LABELER NAME: Camber Pharmaceuticals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 20(mg/1)
START MARKETING DATE: 2016-08-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 31722-581_6ec41372-223f-40e0-b376-a3a4faa0a5d1
PRODUCT NDC: 31722-581
APPLICATION NUMBER: ANDA204343

Other DULOXETINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Camber Pharmaceuticals, Inc.Duloxetine