DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PLENDIL
FDA Application No:
(NDA) 019834
Active Ingredient(s):
FELODIPINE
Company:
ASTRAZENECA
Original Approval or Tentative Approval Date:
July 25, 1991
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
PLENDIL
FELODIPINE
5MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
AB
PLENDIL
FELODIPINE
10MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
Yes
AB
PLENDIL
FELODIPINE
2.5MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
AB
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