DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FELODIPINE
FDA Application No:
(ANDA) 075896
Active Ingredient(s):
FELODIPINE
Company:
MUTUAL PHARM
Original Approval or Tentative Approval Date:
November 2, 2004
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
FELODIPINE
FELODIPINE
2.5MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
AB
FELODIPINE
FELODIPINE
5MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
AB
FELODIPINE
FELODIPINE
10MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
AB
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