DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
MECLOMEN
FDA Application No:
(NDA) 018006
Active Ingredient(s):
MECLOFENAMATE SODIUM
Company:
PARKE DAVIS
Original Approval or Tentative Approval Date:
June 25, 1980
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
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
MECLOMEN
MECLOFENAMATE SODIUM
EQ 50MG BASE
CAPSULE; ORAL
Discontinued
No
None
MECLOMEN
MECLOFENAMATE SODIUM
EQ 100MG BASE
CAPSULE; ORAL
Discontinued
No
None
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