DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CARMOL HC
FDA Application No:
(ANDA) 080505
Active Ingredient(s):
HYDROCORTISONE ACETATE; UREA
Company:
KENWOOD LABS
Label History
Labels are not available on this site for CARMOL HC, (ANDA) 080505
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/27/1992
018
Labeling in Effect
11/23/1990
017
Chemistry in Effect
2/5/1990
016
Chemistry
1/12/1973
000
Approval
There are no Therapeutic Equivalents
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