Details for New Drug Application (NDA): 214047
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NDA 214047 describes THYQUIDITY, which is a drug marketed by Azurity and is included in one NDA. It is available from one supplier. There is one patent protecting this drug. Additional details are available on the THYQUIDITY profile page.
The generic ingredient in THYQUIDITY is levothyroxine sodium. There are ten drug master file entries for this compound. Fifty-one suppliers are listed for this compound. Additional details are available on the levothyroxine sodium profile page.
The generic ingredient in THYQUIDITY is levothyroxine sodium. There are ten drug master file entries for this compound. Fifty-one suppliers are listed for this compound. Additional details are available on the levothyroxine sodium profile page.
Summary for 214047
| Tradename: | THYQUIDITY |
| Applicant: | Azurity |
| Ingredient: | levothyroxine sodium |
| Patents: | 1 |
Suppliers and Packaging for NDA: 214047
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| THYQUIDITY | levothyroxine sodium | SOLUTION;ORAL | 214047 | NDA | Azurity Pharmaceuticals, Inc. | 52652-1950 | 52652-1950-1 | 1 BOTTLE, GLASS in 1 CARTON (52652-1950-1) / 100 mL in 1 BOTTLE, GLASS |
| THYQUIDITY | levothyroxine sodium | SOLUTION;ORAL | 214047 | NDA | Azurity Pharmaceuticals, Inc. | 52652-1950 | 52652-1950-2 | 2 CARTON in 1 CARTON (52652-1950-2) / 1 BOTTLE, GLASS in 1 CARTON / 100 mL in 1 BOTTLE, GLASS |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 100MCG/5ML | ||||
| Approval Date: | Nov 30, 2020 | TE: | RLD: | Yes | |||||
| Patent: | ⤷ Sign Up | Patent Expiration: | Aug 6, 2031 | Product Flag? | Y | Substance Flag? | Delist Request? | ||
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