Alfentanil Hydrochloride (Akorn, Inc.)


Welcome to the PulseAid listing for the Alfentanil Hydrochloride drug offered from Akorn, 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: Akorn, 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
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2010-02-01
END MARKETING DATE: 0000-00-00


Alfentanil Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAlfentanil Hydrochloride from Akorn, Inc.
LABELER NAME: Akorn, Inc.
DEA SCHEDULE: CII
ACTIVE STRENGTH: 500(ug/mL)
START MARKETING DATE: 2010-02-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 17478-067_de97cb79-8cf6-46a6-a4be-e108895f97f9
PRODUCT NDC: 17478-067
APPLICATION NUMBER: NDA019353

Other ALFENTANIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Akorn, Inc.Alfentanil Hydrochloride
Hospira, Inc.Alfentanil Hydrochloride