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:
