etomidate (Zydus Pharmaceuticals (USA) Inc.)
Welcome to the PulseAid listing for the etomidate drug offered from Zydus Pharmaceuticals (USA) Inc.. This General Anesthesia [PE],General Anesthetic [EPC] 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: | etomidate |
| SUBSTANCE NAME: | ETOMIDATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | General Anesthesia [PE],General Anesthetic [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2015-04-03 |
| END MARKETING DATE: | 0000-00-00 |
etomidate HUMAN PRESCRIPTION DRUG Details:
| Item Description | etomidate from Zydus Pharmaceuticals (USA) Inc. |
| LABELER NAME: | Zydus Pharmaceuticals (USA) Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2(mg/mL) |
| START MARKETING DATE: | 2015-04-03 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68382-545_e01df60d-670d-44dd-93e3-d4720d210eec |
| PRODUCT NDC: | 68382-545 |
| APPLICATION NUMBER: | ANDA202360 |
Other ETOMIDATE Pharmaceutical Manufacturers / Labelers:
