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: |
|
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: