DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CARDENE
FDA Application No:
(NDA) 019488
Active Ingredient(s):
NICARDIPINE HYDROCHLORIDE
Company:
PDL BIOPHARMA INC
Original Approval or Tentative Approval Date:
December 21, 1988
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
Therapeutic Equivalents
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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
CARDENE
NICARDIPINE HYDROCHLORIDE
20MG
CAPSULE; ORAL
Prescription
No
AB
CARDENE
NICARDIPINE HYDROCHLORIDE
30MG
CAPSULE; ORAL
Prescription
Yes
AB
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