DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DILTIAZEM HYDROCHLORIDE
FDA Application No:
(ANDA) 075375
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
APOTEX INC
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 075375
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/26/2002
002
Microbiology
9/21/2001
001
Microbiology
9/30/1999
000
Approval
Letter
Therapeutic Equivalents
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