Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 076752
Company: MERCK KGAA

Products on ANDA 076752

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.025MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.05MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.075MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.088MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.1MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.112MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.125MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.15MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.175MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.2MG	TABLET;ORAL	Discontinued	None	No	No
LEVOTHYROXINE SODIUM	LEVOTHYROXINE SODIUM	0.3MG	TABLET;ORAL	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 076752

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
06/16/2005	ORIG-1	Approval				Label is not available on this site.

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
10/31/2008	SUPPL-6	Labeling		Label is not available on this site.
09/19/2006	SUPPL-2	Labeling		Label is not available on this site.