DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
LEVOTHYROXINE SODIUM
FDA Application No:
(ANDA) 076764
Active Ingredient(s):
LEVOTHYROXINE SODIUM
Company:
MYLAN
Original Approval or Tentative Approval Date:
June 23, 2004
There are no Therapeutic Equivalents
Labels are not available
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
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.025MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.050MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.075MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.088MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.1MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.112MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.125MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.15MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.175MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.2MG
TABLET; ORAL
Discontinued
No
None
LEVOTHYROXINE SODIUM
LEVOTHYROXINE SODIUM
0.3MG
TABLET; ORAL
Discontinued
No
None
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