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) 074943
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
TORPHARM
Original Approval or Tentative Approval Date:
August 6, 1998
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
240MG
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
No
AB2
DILTIAZEM HYDROCHLORIDE
DILTIAZEM HYDROCHLORIDE
180MG
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
No
AB2
DILTIAZEM HYDROCHLORIDE
DILTIAZEM HYDROCHLORIDE
120MG
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
No
AB2
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