Repaglinide (Paddock Laboratories, LLC)
Welcome to the PulseAid listing for the Repaglinide drug offered from Paddock Laboratories, LLC. This Glinide [EPC],Potassium Channel Antagonists [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: | Paddock Laboratories, LLC |
NON-PROPRIETARY NAME: | REPAGLINIDE |
SUBSTANCE NAME: | REPAGLINIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Glinide [EPC],Potassium Channel Antagonists [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2013-08-09 |
END MARKETING DATE: | 0000-00-00 |
Repaglinide HUMAN PRESCRIPTION DRUG Details:
Item Description | Repaglinide from Paddock Laboratories, LLC |
LABELER NAME: | Paddock Laboratories, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.5(mg/1) |
START MARKETING DATE: | 2013-08-09 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0574-0240_e5bfb401-a51b-4a08-9a43-a9b640250323 |
PRODUCT NDC: | 0574-0240 |
APPLICATION NUMBER: | ANDA201189 |
Other REPAGLINIDE Pharmaceutical Manufacturers / Labelers: