DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DDAVP
FDA Application No:
(NDA) 018938
Active Ingredient(s):
DESMOPRESSIN ACETATE
Company:
SANOFI AVENTIS US
Original Approval or Tentative Approval Date:
March 30, 1984
Chemical Type:
3 New dosage form
Review Classification:
P Priority review drug
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
DDAVP
DESMOPRESSIN ACETATE
0.004MG/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
DDAVP
DESMOPRESSIN ACETATE
0.015MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
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