Search results from the "OB_Rx" table for query
on "076752."
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.025MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
001 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.05MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
002 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.075MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
003 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.088MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
004 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.1MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
005 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.112MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
006 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.125MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
007 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.15MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
008 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.175MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
009 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.2MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
010 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
LEVOTHYROXINE SODIUM |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
LEVOTHYROXINE SODIUM |
| Applicant: |
MERCK KGAA |
| Strength: |
0.3MG **See 2008 Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium |
| Application Number: |
A076752 |
| Product Number: |
011 |
| Approval Date: |
Jun 16, 2005 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB2,AB3 |
| Patent and Exclusivity Info for this product: |
View |
|
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Office of Generic Drugs
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Division of Labeling and Program Support
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Generic Drug Product Information & Patent Information - Daily
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Orange Book Data Updated Through December, 2009
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Patent and Generic Drug Product Data Last Updated: February 04, 2010
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