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 Description | Duloxetine from Camber Pharmaceuticals, Inc. |
LABELER NAME: | Camber Pharmaceuticals, Inc. |
DEA SCHEDULE: |
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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: