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) 020755
Active Ingredient(s):
ALPROSTADIL
Company:
PFIZER
Original Approval or Tentative Approval Date:
October 31, 1997
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
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
CAVERJECT
ALPROSTADIL
0.005MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
CAVERJECT
ALPROSTADIL
0.01MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
CAVERJECT
ALPROSTADIL
0.02MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
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