DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
MOMETASONE
FDA Application No:
(ANDA) 077678
Active Ingredient(s):
MOMETASONE FUROATE
Company:
G AND W LABS
Original Approval or Tentative Approval Date:
March 7, 2006
There are no Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
MOMETASONE
MOMETASONE FUROATE
0.1%
LOTION; TOPICAL
Tentative Approval
No
None
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