Repaglinide (Sun Pharmaceutical Industries, Inc.)
Welcome to the PulseAid listing for the Repaglinide drug offered from Sun Pharmaceutical Industries, Inc.. 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: | Sun Pharmaceutical Industries, Inc. |
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: | 2013-07-11 |
END MARKETING DATE: | 0000-00-00 |
Repaglinide HUMAN PRESCRIPTION DRUG Details:
Item Description | Repaglinide from Sun Pharmaceutical Industries, Inc. |
LABELER NAME: | Sun Pharmaceutical Industries, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1(mg/1) |
START MARKETING DATE: | 2013-07-11 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 57664-745_29140632-9c39-4f89-9b96-908099e6b48c |
PRODUCT NDC: | 57664-745 |
APPLICATION NUMBER: | ANDA077571 |
Other REPAGLINIDE Pharmaceutical Manufacturers / Labelers: