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fentanyl citrate - 55253-070-30 - (fentanyl citrate)

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Drug Information of fentanyl citrate

Product NDC: 55253-070
Proprietary Name: fentanyl citrate
Non Proprietary Name: fentanyl citrate
Active Ingredient(s): 200    ug/1 & nbsp;   fentanyl citrate
Administration Route(s): TRANSMUCOSAL
Dosage Form(s): LOZENGE
Coding System: National Drug Codes(NDC)

Labeler Information of fentanyl citrate

Product NDC: 55253-070
Labeler Name: CIMA Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020747
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20060906

Package Information of fentanyl citrate

Package NDC: 55253-070-30
Package Description: 10 BLISTER PACK in 1 CARTON (55253-070-30) > 3 LOZENGE in 1 BLISTER PACK (55253-070-01)

NDC Information of fentanyl citrate

NDC Code 55253-070-30
Proprietary Name fentanyl citrate
Package Description 10 BLISTER PACK in 1 CARTON (55253-070-30) > 3 LOZENGE in 1 BLISTER PACK (55253-070-01)
Product NDC 55253-070
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl citrate
Dosage Form Name LOZENGE
Route Name TRANSMUCOSAL
Start Marketing Date 20060906
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name CIMA Laboratories, Inc.
Substance Name FENTANYL CITRATE
Strength Number 200
Strength Unit ug/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of fentanyl citrate


General Information