DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ADALAT CC
FDA Application No:
(NDA) 020198
Active Ingredient(s):
NIFEDIPINE
Company:
BAYER PHARMS
Original Approval or Tentative Approval Date:
April 21, 1993
Chemical Type:
5 New manufacturer
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
ADALAT CC
NIFEDIPINE
30MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
No
AB1
ADALAT CC
NIFEDIPINE
60MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
Yes
AB1
ADALAT CC
NIFEDIPINE
90MG
TABLET, EXTENDED RELEASE; ORAL
Prescription
Yes
AB1
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