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) 076705
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
DR REDDYS LABS INC
Label History
Labels are not available on this site for RANITIDINE HYDROCHLORIDE, (ANDA) 076705
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/27/2005
000
Approval
Therapeutic Equivalents
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