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Details for New Drug Application (NDA): 070637

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NDA 070637 describes FENTANYL CITRATE, which is a drug marketed by Mallinckrodt, Par Pharm, Hospira, Abbott, Watson Labs, Astrazeneca, West-ward Pharms Int, and Watson Labs Inc, and is included in fourteen NDAs. It is available from five suppliers. Additional details are available on the FENTANYL CITRATE profile page.

The generic ingredient in FENTANYL CITRATE is droperidol; fentanyl citrate. There are five drug master file entries for this compound. Additional details are available on the droperidol; fentanyl citrate profile page.

Summary for NDA: 070637

Tradename:
FENTANYL CITRATE
Applicant:
Abbott
Ingredient:
fentanyl citrate
Patents:0
Therapeutic Class:Analgesics
Formulation / Manufacturing:see details

Summary for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrengthEQ 0.05MG BASE/ML
Approval Date:Apr 30, 1990TE:RLD:No


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