PROPOFOL (Hospira, Inc.)
Welcome to the PulseAid listing for the PROPOFOL drug offered from Hospira, Inc.. This General Anesthesia [PE],General Anesthetic [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view the 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: | PROPOFOL |
| SUBSTANCE NAME: | PROPOFOL |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | General Anesthesia [PE],General Anesthetic [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, EMULSION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2006-04-03 |
| END MARKETING DATE: | 0000-00-00 |
PROPOFOL HUMAN PRESCRIPTION DRUG Details:
| Item Description | PROPOFOL from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 2006-04-03 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-4699_2479b268-34ce-493b-aa23-ebfe27d922aa |
| PRODUCT NDC: | 0409-4699 |
| APPLICATION NUMBER: | ANDA077908 |
Other PROPOFOL Pharmaceutical Manufacturers / Labelers:
