DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
HIPREX
FDA Application No:
(NDA) 017681
Active Ingredient(s):
METHENAMINE HIPPURATE
Company:
SANOFI AVENTIS US
Original Approval or Tentative Approval Date:
September 9, 1976
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
HIPREX
METHENAMINE HIPPURATE
1GM
TABLET; ORAL
Prescription
Yes
AB
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