DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NIFEDIPINE
FDA Application No:
(ANDA) 072556
Active Ingredient(s):
NIFEDIPINE
Company:
ACTAVIS ELIZABETH
Original Approval or Tentative Approval Date:
April 28, 1989
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
NIFEDIPINE
NIFEDIPINE
20MG
CAPSULE; ORAL
Prescription
No
AB
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