DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SANDRIL
FDA Application No:
(NDA) 010012
Active Ingredient(s):
RESERPINE
Company:
LILLY
Label History
Labels are not available on this site for SANDRIL, (NDA) 010012
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/20/1983
006
Labeling Revision
10/22/1981
004
Manufacturing Change or Addition
Therapeutic Equivalents
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