DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FENTORA
FDA Application No:
(NDA) 021947
Active Ingredient(s):
FENTANYL CITRATE
Company:
CEPHALON
Original Approval or Tentative Approval Date:
September 25, 2006
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
FENTORA
FENTANYL CITRATE
EQ 0.1MG BASE
TABLET; BUCCAL
Prescription
No
None
FENTORA
FENTANYL CITRATE
EQ 0.2MG BASE
TABLET; BUCCAL
Prescription
No
None
FENTORA
FENTANYL CITRATE
EQ 0.4MG BASE
TABLET; BUCCAL
Prescription
Yes
None
FENTORA
FENTANYL CITRATE
EQ 0.6MG BASE
TABLET; BUCCAL
Prescription
No
None
FENTORA
FENTANYL CITRATE
EQ 0.8MG BASE
TABLET; BUCCAL
Prescription
No
None
FENTORA
FENTANYL CITRATE
EQ 0.3MG BASE
TABLET; BUCCAL
Prescription
No
None
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