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Fentanyl Citrate - 52533-074-15 - (Fentanyl Citrate)

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Drug Information of Fentanyl Citrate

Product NDC: 52533-074
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: 52533-074
Labeler Name: Cantrell Drug Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20111020

Package Information of Fentanyl Citrate

Package NDC: 52533-074-15
Package Description: 5 mL in 1 SYRINGE (52533-074-15)

NDC Information of Fentanyl Citrate

NDC Code 52533-074-15
Proprietary Name Fentanyl Citrate
Package Description 5 mL in 1 SYRINGE (52533-074-15)
Product NDC 52533-074
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl Citrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20111020
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Cantrell Drug Company
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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