DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DESMOPRESSIN ACETATE
FDA Application No:
(ANDA) 075220
Active Ingredient(s):
DESMOPRESSIN ACETATE
Company:
HOSPIRA
Original Approval or Tentative Approval Date:
August 28, 2000
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
DESMOPRESSIN ACETATE
DESMOPRESSIN ACETATE
0.004MG/ML
INJECTABLE; INJECTION
Prescription
No
AP
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