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Alfentanil Hydrochloride - 0409-2266-49 - (ALFENTANIL HYDROCHLORIDE)

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Drug Information of Alfentanil Hydrochloride

Product NDC: 0409-2266
Proprietary Name: Alfentanil Hydrochloride
Non Proprietary Name: ALFENTANIL HYDROCHLORIDE
Active Ingredient(s): 500    ug/mL & nbsp;   ALFENTANIL HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Alfentanil Hydrochloride

Product NDC: 0409-2266
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075221
Marketing Category: ANDA
Start Marketing Date: 20111010

Package Information of Alfentanil Hydrochloride

Package NDC: 0409-2266-49
Package Description: 10 AMPULE in 1 CARTON (0409-2266-49) > 2 mL in 1 AMPULE

NDC Information of Alfentanil Hydrochloride

NDC Code 0409-2266-49
Proprietary Name Alfentanil Hydrochloride
Package Description 10 AMPULE in 1 CARTON (0409-2266-49) > 2 mL in 1 AMPULE
Product NDC 0409-2266
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALFENTANIL HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20111010
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name ALFENTANIL HYDROCHLORIDE
Strength Number 500
Strength Unit ug/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Alfentanil Hydrochloride


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