DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FENOPROFEN CALCIUM
FDA Application No:
(ANDA) 072437
Active Ingredient(s):
FENOPROFEN CALCIUM
Company:
PAR PHARM
Original Approval or Tentative Approval Date:
August 22, 1988
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
FENOPROFEN CALCIUM
FENOPROFEN CALCIUM
EQ 200MG BASE
CAPSULE; ORAL
Prescription
No
AB
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