Propofol (APP Pharmaceuticals, LLC)
Welcome to the PulseAid listing for the Propofol drug offered from APP Pharmaceuticals, LLC. 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: | APP Pharmaceuticals, LLC |
| 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: | NDA |
| START MARKETING DATE: | 2009-10-23 |
| END MARKETING DATE: | 0000-00-00 |
Propofol HUMAN PRESCRIPTION DRUG Details:
| Item Description | Propofol from APP Pharmaceuticals, LLC |
| LABELER NAME: | APP Pharmaceuticals, LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 2009-10-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63323-270_454ceeef-5f00-4da6-9236-b17c7bbf656c |
| PRODUCT NDC: | 63323-270 |
| APPLICATION NUMBER: | NDA019627 |
Other PROPOFOL Pharmaceutical Manufacturers / Labelers:
