DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
LASIX
FDA Application No:
(NDA) 016273
Active Ingredient(s):
FUROSEMIDE
Company:
SANOFI AVENTIS US
Original Approval or Tentative Approval Date:
July 1, 1966
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
LASIX
FUROSEMIDE
40MG
TABLET; ORAL
Prescription
No
AB
LASIX
FUROSEMIDE
20MG
TABLET; ORAL
Prescription
No
AB
LASIX
FUROSEMIDE
80MG
TABLET; ORAL
Prescription
Yes
AB
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