DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
RANITIDINE HYDROCHLORIDE
FDA Application No:
(ANDA) 077824
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
INTERPHARM
Label History
Labels are not available on this site for RANITIDINE HYDROCHLORIDE, (ANDA) 077824
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/13/2006
000
Approval
Therapeutic Equivalents
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