DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NALOXONE HYDROCHLORIDE
FDA Application No:
(ANDA) 070417
Active Ingredient(s):
NALOXONE HYDROCHLORIDE
Company:
INTL MEDICATION
Label History
Labels are not available on this site for NALOXONE HYDROCHLORIDE, (ANDA) 070417
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/29/1988
006
Chemistry
5/20/1988
005
Labeling
11/29/1988
004
Chemistry
Therapeutic Equivalents
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