Details for New Drug Application (NDA): 211369
The generic ingredient in LEVOTHYROXINE SODIUM is levothyroxine sodium. There is one drug master file entry for this compound. Fifty suppliers are listed for this compound. Additional details are available on the levothyroxine sodium profile page.
Summary for 211369
| Tradename: | LEVOTHYROXINE SODIUM |
| Applicant: | Ani Pharms |
| Ingredient: | levothyroxine sodium |
| Patents: | 0 |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | 0.075MG | ||||
| Approval Date: | Oct 28, 2020 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | 0.15MG | ||||
| Approval Date: | Oct 28, 2020 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | 0.112MG | ||||
| Approval Date: | Apr 16, 2021 | TE: | RLD: | No | |||||
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