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) 075749
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
INTL MEDICATION
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 075749
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/27/2002
001
Control Supplement
11/21/2001
000
Approval
Letter
Therapeutic Equivalents
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