DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CAVERJECT
FDA Application No:
(NDA) 020379
Active Ingredient(s):
ALPROSTADIL
Company:
PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date:
July 6, 1995
Chemical Type:
3 New dosage form
Review Classification:
P Priority review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
CAVERJECT
ALPROSTADIL
0.01MG/VIAL
INJECTABLE; INJECTION
Prescription
No
AP
CAVERJECT
ALPROSTADIL
0.02MG/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
CAVERJECT
ALPROSTADIL
0.005MG/VIAL
INJECTABLE; INJECTION
Prescription
No
None
CAVERJECT
ALPROSTADIL
0.04MG/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
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