Alfentanil Hydrochloride (Hospira, Inc.)
Welcome to the PulseAid listing for the Alfentanil Hydrochloride drug offered from Hospira, Inc.. This Full Opioid Agonists [MoA],Opioid Agonist [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: | Alfentanil Hydrochloride |
| SUBSTANCE NAME: | ALFENTANIL HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2006-02-20 |
| END MARKETING DATE: | 0000-00-00 |
Alfentanil Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Alfentanil Hydrochloride from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 500(ug/mL) |
| START MARKETING DATE: | 2006-02-20 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-2266_bcbe32e9-5795-4a2b-b3df-53340c34390a |
| PRODUCT NDC: | 0409-2266 |
| APPLICATION NUMBER: | ANDA075221 |
Other ALFENTANIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
