DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
JANTOVEN
FDA Application No:
(NDA) 040416
Active Ingredient(s):
WARFARIN SODIUM
Company:
USL PHARMA
Original Approval or Tentative Approval Date:
October 2, 2003
Therapeutic Equivalents
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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
JANTOVEN
WARFARIN SODIUM
1MG
TABLET; ORAL
Prescription
No
AB
JANTOVEN
WARFARIN SODIUM
2MG
TABLET; ORAL
Prescription
No
AB
JANTOVEN
WARFARIN SODIUM
2.5MG
TABLET; ORAL
Prescription
No
AB
JANTOVEN
WARFARIN SODIUM
3MG
TABLET; ORAL
Prescription
No
AB
JANTOVEN
WARFARIN SODIUM
4MG
TABLET; ORAL
Prescription
No
AB
JANTOVEN
WARFARIN SODIUM
5MG
TABLET; ORAL
Prescription
No
AB
JANTOVEN
WARFARIN SODIUM
6MG
TABLET; ORAL
Prescription
No
AB
JANTOVEN
WARFARIN SODIUM
7.5MG
TABLET; ORAL
Prescription
No
AB
JANTOVEN
WARFARIN SODIUM
10MG
TABLET; ORAL
Prescription
No
AB
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