Nateglinide (Zydus Pharmaceuticals (USA) Inc.)
Welcome to the PulseAid listing for the Nateglinide drug offered from Zydus Pharmaceuticals (USA) 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: | Zydus Pharmaceuticals (USA) Inc. |
| NON-PROPRIETARY NAME: | Nateglinide |
| SUBSTANCE NAME: | NATEGLINIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Glinide [EPC],Potassium Channel Antagonists [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-10-27 |
| END MARKETING DATE: | 0000-00-00 |
Nateglinide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Nateglinide from Zydus Pharmaceuticals (USA) Inc. |
| LABELER NAME: | Zydus Pharmaceuticals (USA) Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 60(mg/1) |
| START MARKETING DATE: | 2016-10-27 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68382-721_a38f6a32-c1ee-43dc-aa96-f7b78e4d5a29 |
| PRODUCT NDC: | 68382-721 |
| APPLICATION NUMBER: | ANDA205248 |
Other NATEGLINIDE Pharmaceutical Manufacturers / Labelers:
