Alfenta - 17478-067-20 - (Alfentanil hydrochloride)

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Drug Information of Alfenta

Product NDC: 17478-067
Proprietary Name: Alfenta
Non Proprietary Name: Alfentanil hydrochloride
Active Ingredient(s): 500    ug/mL & nbsp;   Alfentanil hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Alfenta

Product NDC: 17478-067
Labeler Name: Akorn
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019353
Marketing Category: NDA
Start Marketing Date: 20100201

Package Information of Alfenta

Package NDC: 17478-067-20
Package Description: 5 AMPULE in 1 CARTON (17478-067-20) > 20 mL in 1 AMPULE

NDC Information of Alfenta

NDC Code 17478-067-20
Proprietary Name Alfenta
Package Description 5 AMPULE in 1 CARTON (17478-067-20) > 20 mL in 1 AMPULE
Product NDC 17478-067
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alfentanil hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20100201
Marketing Category Name NDA
Labeler Name Akorn
Substance Name ALFENTANIL HYDROCHLORIDE
Strength Number 500
Strength Unit ug/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Alfenta


General Information