DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FENTANYL-25
FDA Application No:
(ANDA) 077062
Active Ingredient(s):
FENTANYL
Company:
ABRIKA PHARMS
Original Approval or Tentative Approval Date:
September 20, 2007
Therapeutic Equivalents
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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
FENTANYL-100
FENTANYL
100UGM/HR
FILM, EXTENDED RELEASE; TRANSDERMAL
Prescription
No
AB
FENTANYL-25
FENTANYL
25UGM/HR
FILM, EXTENDED RELEASE; TRANSDERMAL
Prescription
No
AB
FENTANYL-50
FENTANYL
50UGM/HR
FILM, EXTENDED RELEASE; TRANSDERMAL
Prescription
No
AB
FENTANYL-75
FENTANYL
75UGM/HR
FILM, EXTENDED RELEASE; TRANSDERMAL
Prescription
No
AB
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