DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CARDIZEM
FDA Application No:
(NDA) 020027
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
BIOVAIL LABS INTL
Original Approval or Tentative Approval Date:
October 24, 1991
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
Therapeutic Equivalents
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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
CARDIZEM
DILTIAZEM HYDROCHLORIDE
5MG/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
CARDIZEM
DILTIAZEM HYDROCHLORIDE
25MG/VIAL
INJECTABLE; INJECTION
Prescription
Yes
None
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