AMIDATE (Hospira, Inc.)
Welcome to the PulseAid listing for the AMIDATE drug offered from Hospira, 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: | Hospira, 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: | NDA |
| START MARKETING DATE: | 2016-01-28 |
| END MARKETING DATE: | 0000-00-00 |
AMIDATE HUMAN PRESCRIPTION DRUG Details:
| Item Description | AMIDATE from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2(mg/mL) |
| START MARKETING DATE: | 2016-01-28 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-6695_19aad568-5dcc-4e11-8d8f-fc26d1a71e9c |
| PRODUCT NDC: | 0409-6695 |
| APPLICATION NUMBER: | NDA018227 |
Other ETOMIDATE Pharmaceutical Manufacturers / Labelers:
