List of Excipients in API ubrogepant
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Excipients in NDA-approved (novel) drugs containing ubrogepant
Company | Tradename | Ingredient | NDC | Excipient | Potential Generic Entry |
---|---|---|---|---|---|
Allergan Inc | UBRELVY | ubrogepant | 0023-6498 | CELLULOSE, MICROCRYSTALLINE | 2035-01-30 |
Allergan Inc | UBRELVY | ubrogepant | 0023-6498 | COPOVIDONE K25-31 | 2035-01-30 |
Allergan Inc | UBRELVY | ubrogepant | 0023-6498 | CROSCARMELLOSE SODIUM | 2035-01-30 |
Allergan Inc | UBRELVY | ubrogepant | 0023-6498 | MANNITOL | 2035-01-30 |
Allergan Inc | UBRELVY | ubrogepant | 0023-6498 | SILICON DIOXIDE | 2035-01-30 |
Allergan Inc | UBRELVY | ubrogepant | 0023-6498 | SODIUM CHLORIDE | 2035-01-30 |
>Company | >Tradename | >Ingredient | >NDC | >Excipient | >Potential Generic Entry |
Detailed excipient profiles for ubrogepant
Excipient focus: CELLULOSE, MICROCRYSTALLINE
ubrogepant drug variants containing CELLULOSE, MICROCRYSTALLINE
Company | Ingredient | NDC |
---|---|---|
Allergan Inc | ubrogepant | 0023-6498 |
>Company | >Ingredient | >NDC |
ubrogepant drug variants not containing CELLULOSE, MICROCRYSTALLINE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: COPOVIDONE K25-31
ubrogepant drug variants containing COPOVIDONE K25-31
Company | Ingredient | NDC |
---|---|---|
Allergan Inc | ubrogepant | 0023-6498 |
>Company | >Ingredient | >NDC |
ubrogepant drug variants not containing COPOVIDONE K25-31
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: CROSCARMELLOSE SODIUM
ubrogepant drug variants containing CROSCARMELLOSE SODIUM
Company | Ingredient | NDC |
---|---|---|
Allergan Inc | ubrogepant | 0023-6498 |
>Company | >Ingredient | >NDC |
ubrogepant drug variants not containing CROSCARMELLOSE SODIUM
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: MANNITOL
ubrogepant drug variants containing MANNITOL
Company | Ingredient | NDC |
---|---|---|
Allergan Inc | ubrogepant | 0023-6498 |
>Company | >Ingredient | >NDC |
ubrogepant drug variants not containing MANNITOL
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: SILICON DIOXIDE
ubrogepant drug variants containing SILICON DIOXIDE
Company | Ingredient | NDC |
---|---|---|
Allergan Inc | ubrogepant | 0023-6498 |
>Company | >Ingredient | >NDC |
ubrogepant drug variants not containing SILICON DIOXIDE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: SODIUM CHLORIDE
ubrogepant drug variants containing SODIUM CHLORIDE
Company | Ingredient | NDC |
---|---|---|
Allergan Inc | ubrogepant | 0023-6498 |
>Company | >Ingredient | >NDC |
ubrogepant drug variants not containing SODIUM CHLORIDE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: SODIUM STEARYL FUMARATE
ubrogepant drug variants containing SODIUM STEARYL FUMARATE
Company | Ingredient | NDC |
---|---|---|
Allergan Inc | ubrogepant | 0023-6498 |
>Company | >Ingredient | >NDC |
ubrogepant drug variants not containing SODIUM STEARYL FUMARATE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: VITAMIN E POLYETHYLENE GLYCOL SUCCINATE
ubrogepant drug variants containing VITAMIN E POLYETHYLENE GLYCOL SUCCINATE
Company | Ingredient | NDC |
---|---|---|
Allergan Inc | ubrogepant | 0023-6498 |
>Company | >Ingredient | >NDC |
ubrogepant drug variants not containing VITAMIN E POLYETHYLENE GLYCOL SUCCINATE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
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