DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEPERIDINE HYDROCHLORIDE
FDA Application No:
(ANDA) 088282
Active Ingredient(s):
MEPERIDINE HYDROCHLORIDE
Company:
BAXTER HLTHCARE
Label History
Labels are not available on this site for MEPERIDINE HYDROCHLORIDE, (ANDA) 088282
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/3/1986
001
Chemistry
6/15/1984
000
Approval
Therapeutic Equivalents
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