DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
RESECTISOL
FDA Application No:
(NDA) 016704
Active Ingredient(s):
MANNITOL
Company:
B BRAUN
Original Approval or Tentative Approval Date:
November 18, 1969
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
RESECTISOL
MANNITOL
5GM/100ML
SOLUTION; IRRIGATION
Discontinued
No
None
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