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Transmucosal Fentanyl Citrate - 52959-566-30 - (fentanyl citrate)

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Drug Information of Transmucosal Fentanyl Citrate

Product NDC: 52959-566
Proprietary Name: Transmucosal Fentanyl Citrate
Non Proprietary Name: fentanyl citrate
Active Ingredient(s): 1200    1/1 & nbsp;   fentanyl citrate
Administration Route(s): ORAL; TRANSMUCOSAL
Dosage Form(s): LOZENGE
Coding System: National Drug Codes(NDC)

Labeler Information of Transmucosal Fentanyl Citrate

Product NDC: 52959-566
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020747
Marketing Category: NDA
Start Marketing Date: 20060906

Package Information of Transmucosal Fentanyl Citrate

Package NDC: 52959-566-30
Package Description: 30 BLISTER PACK in 1 CARTON (52959-566-30) > 1 LOZENGE in 1 BLISTER PACK (52959-566-01)

NDC Information of Transmucosal Fentanyl Citrate

NDC Code 52959-566-30
Proprietary Name Transmucosal Fentanyl Citrate
Package Description 30 BLISTER PACK in 1 CARTON (52959-566-30) > 1 LOZENGE in 1 BLISTER PACK (52959-566-01)
Product NDC 52959-566
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl citrate
Dosage Form Name LOZENGE
Route Name ORAL; TRANSMUCOSAL
Start Marketing Date 20060906
Marketing Category Name NDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name FENTANYL CITRATE
Strength Number 1200
Strength Unit 1/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Transmucosal Fentanyl Citrate


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