DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NEBUPENT
FDA Application No:
(NDA) 019887
Active Ingredient(s):
PENTAMIDINE ISETHIONATE
Company:
ABRAXIS PHARM
Original Approval or Tentative Approval Date:
June 15, 1989
Chemical Type:
3 New dosage form
Review Classification:
P Priority review drug
O Orphan drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
NEBUPENT
PENTAMIDINE ISETHIONATE
300MG/VIAL
FOR SOLUTION; INHALATION
Prescription
Yes
None
NEBUPENT
PENTAMIDINE ISETHIONATE
600MG/VIAL
FOR SOLUTION; INHALATION
Prescription
No
None
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