Details for New Drug Application (NDA): 076752
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The generic ingredient in LEVOTHYROXINE SODIUM is levothyroxine sodium. There are ten drug master file entries for this compound. Fifty-three suppliers are listed for this compound. Additional details are available on the levothyroxine sodium profile page.
Summary for 076752
| Tradename: | LEVOTHYROXINE SODIUM |
| Applicant: | Merck Kgaa |
| Ingredient: | levothyroxine sodium |
| Patents: | 0 |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 0.025MG | ||||
| Approval Date: | Jun 16, 2005 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 0.05MG | ||||
| Approval Date: | Jun 16, 2005 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 0.075MG | ||||
| Approval Date: | Jun 16, 2005 | TE: | RLD: | No | |||||
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