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FENTANYL CITRATE - 52533-024-71 - (FENTANYL CITRATE)

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Drug Information of FENTANYL CITRATE

Product NDC: 52533-024
Proprietary Name: FENTANYL CITRATE
Non Proprietary Name: FENTANYL CITRATE
Active Ingredient(s): 10    ug/mL & nbsp;   FENTANYL CITRATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of FENTANYL CITRATE

Product NDC: 52533-024
Labeler Name: Cantrell Drug Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120413

Package Information of FENTANYL CITRATE

Package NDC: 52533-024-71
Package Description: 100 mL in 1 BAG (52533-024-71)

NDC Information of FENTANYL CITRATE

NDC Code 52533-024-71
Proprietary Name FENTANYL CITRATE
Package Description 100 mL in 1 BAG (52533-024-71)
Product NDC 52533-024
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FENTANYL CITRATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120413
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Cantrell Drug Company
Substance Name FENTANYL CITRATE
Strength Number 10
Strength Unit ug/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of FENTANYL CITRATE


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