DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
MECLOFENAMATE SODIUM
FDA Application No:
(ANDA) 071469
Active Ingredient(s):
MECLOFENAMATE SODIUM
Company:
WATSON LABS
Original Approval or Tentative Approval Date:
April 15, 1987
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
MECLOFENAMATE SODIUM
MECLOFENAMATE SODIUM
EQ 100MG BASE
CAPSULE; ORAL
Prescription
No
AB
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