DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DILTIAZEM HYDROCHLORIDE
FDA Application No:
(ANDA) 074845
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
BIOVAIL
Original Approval or Tentative Approval Date:
September 15, 1999
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
DILTIAZEM HYDROCHLORIDE
DILTIAZEM HYDROCHLORIDE
60MG
CAPSULE, EXTENDED RELEASE; ORAL
Discontinued
No
None
DILTIAZEM HYDROCHLORIDE
DILTIAZEM HYDROCHLORIDE
90MG
CAPSULE, EXTENDED RELEASE; ORAL
Discontinued
No
None
DILTIAZEM HYDROCHLORIDE
DILTIAZEM HYDROCHLORIDE
120MG
CAPSULE, EXTENDED RELEASE; ORAL
Discontinued
No
None
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