Etomidate (American Regent, Inc.)
Welcome to the PulseAid listing for the Etomidate drug offered from American Regent, 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: | American Regent, 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: | 2010-06-30 |
| END MARKETING DATE: | 0000-00-00 |
Etomidate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Etomidate from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2(mg/mL) |
| START MARKETING DATE: | 2010-06-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-0780_6229ff97-532b-4c62-9d19-ed22c952f5f8 |
| PRODUCT NDC: | 0517-0780 |
| APPLICATION NUMBER: | ANDA078867 |
Other ETOMIDATE Pharmaceutical Manufacturers / Labelers:
