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Fentanyl Citrate - 0409-9093-32 - (FENTANYL CITRATE)

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Drug Information of Fentanyl Citrate

Product NDC: 0409-9093
Proprietary Name: Fentanyl Citrate
Non Proprietary Name: FENTANYL CITRATE
Active Ingredient(s): 50    ug/mL & nbsp;   FENTANYL CITRATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl Citrate

Product NDC: 0409-9093
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019115
Marketing Category: NDA
Start Marketing Date: 20111123

Package Information of Fentanyl Citrate

Package NDC: 0409-9093-32
Package Description: 10 AMPULE in 1 PACKAGE (0409-9093-32) > 2 mL in 1 AMPULE

NDC Information of Fentanyl Citrate

NDC Code 0409-9093-32
Proprietary Name Fentanyl Citrate
Package Description 10 AMPULE in 1 PACKAGE (0409-9093-32) > 2 mL in 1 AMPULE
Product NDC 0409-9093
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FENTANYL CITRATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20111123
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name FENTANYL CITRATE
Strength Number 50
Strength Unit ug/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl Citrate


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