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Sufentanil Citrate - 0409-3380-35 - (SUFENTANIL CITRATE)

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Drug Information of Sufentanil Citrate

Product NDC: 0409-3380
Proprietary Name: Sufentanil Citrate
Non Proprietary Name: SUFENTANIL CITRATE
Active Ingredient(s): 50    ug/mL & nbsp;   SUFENTANIL CITRATE
Administration Route(s): EPIDURAL; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sufentanil Citrate

Product NDC: 0409-3380
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074534
Marketing Category: ANDA
Start Marketing Date: 20111011

Package Information of Sufentanil Citrate

Package NDC: 0409-3380-35
Package Description: 10 AMPULE in 1 CONTAINER (0409-3380-35) > 5 mL in 1 AMPULE

NDC Information of Sufentanil Citrate

NDC Code 0409-3380-35
Proprietary Name Sufentanil Citrate
Package Description 10 AMPULE in 1 CONTAINER (0409-3380-35) > 5 mL in 1 AMPULE
Product NDC 0409-3380
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SUFENTANIL CITRATE
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; INTRAVENOUS
Start Marketing Date 20111011
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name SUFENTANIL CITRATE
Strength Number 50
Strength Unit ug/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Sufentanil Citrate


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