DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROPOXYPHENE HYDROCHLORIDE
FDA Application No:
(ANDA) 083186
Active Ingredient(s):
PROPOXYPHENE HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for PROPOXYPHENE HYDROCHLORIDE, (ANDA) 083186
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
045
Chemistry
12/23/1994
044
Chemistry
4/3/1992
043
Chemistry
4/3/1992
041
Chemistry
4/10/1987
040
Chemistry
12/18/1972
000
Approval
Therapeutic Equivalents
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