DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
RECLAST
FDA Application No:
(NDA) 021817
Active Ingredient(s):
ZOLEDRONIC ACID
Company:
NOVARTIS
Original Approval or Tentative Approval Date:
April 16, 2007
Chemical Type:
3 New dosage form
Review Classification:
P Priority review drug
There are no 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
RECLAST
ZOLEDRONIC ACID
EQ 5MG BASE/100ML
INJECTABLE; IV (INFUSION)
Prescription
Yes
None
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On
Saturday, July 19, 2014
ariadni psillos
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MLG2OJ
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