List of Excipients in API ZANUBRUTINIB
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Excipients in NDA-approved (novel) drugs containing ZANUBRUTINIB
Company | Tradename | Ingredient | NDC | Excipient | Potential Generic Entry |
---|---|---|---|---|---|
BEIGENE USA INC | BRUKINSA | zanubrutinib | 72579-011 | CELLULOSE, MICROCRYSTALLINE | 2037-08-15 |
BEIGENE USA INC | BRUKINSA | zanubrutinib | 72579-011 | CROSCARMELLOSE SODIUM | 2037-08-15 |
BEIGENE USA INC | BRUKINSA | zanubrutinib | 72579-011 | FERROSOFERRIC OXIDE | 2037-08-15 |
>Company | >Tradename | >Ingredient | >NDC | >Excipient | >Potential Generic Entry |
Detailed excipient profiles for ZANUBRUTINIB
Excipient focus: CELLULOSE, MICROCRYSTALLINE
ZANUBRUTINIB drug variants containing CELLULOSE, MICROCRYSTALLINE
Company | Ingredient | NDC |
---|---|---|
BEIGENE USA INC | zanubrutinib | 72579-011 |
>Company | >Ingredient | >NDC |
ZANUBRUTINIB drug variants not containing CELLULOSE, MICROCRYSTALLINE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: CROSCARMELLOSE SODIUM
ZANUBRUTINIB drug variants containing CROSCARMELLOSE SODIUM
Company | Ingredient | NDC |
---|---|---|
BEIGENE USA INC | zanubrutinib | 72579-011 |
>Company | >Ingredient | >NDC |
ZANUBRUTINIB drug variants not containing CROSCARMELLOSE SODIUM
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: FERROSOFERRIC OXIDE
ZANUBRUTINIB drug variants containing FERROSOFERRIC OXIDE
Company | Ingredient | NDC |
---|---|---|
BEIGENE USA INC | zanubrutinib | 72579-011 |
>Company | >Ingredient | >NDC |
ZANUBRUTINIB drug variants not containing FERROSOFERRIC OXIDE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: GELATIN
ZANUBRUTINIB drug variants containing GELATIN
Company | Ingredient | NDC |
---|---|---|
BEIGENE USA INC | zanubrutinib | 72579-011 |
>Company | >Ingredient | >NDC |
ZANUBRUTINIB drug variants not containing GELATIN
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: MAGNESIUM STEARATE
ZANUBRUTINIB drug variants containing MAGNESIUM STEARATE
Company | Ingredient | NDC |
---|---|---|
BEIGENE USA INC | zanubrutinib | 72579-011 |
>Company | >Ingredient | >NDC |
ZANUBRUTINIB drug variants not containing MAGNESIUM STEARATE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: SILICON DIOXIDE
ZANUBRUTINIB drug variants containing SILICON DIOXIDE
Company | Ingredient | NDC |
---|---|---|
BEIGENE USA INC | zanubrutinib | 72579-011 |
>Company | >Ingredient | >NDC |
ZANUBRUTINIB drug variants not containing SILICON DIOXIDE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: SODIUM LAURYL SULFATE
ZANUBRUTINIB drug variants containing SODIUM LAURYL SULFATE
Company | Ingredient | NDC |
---|---|---|
BEIGENE USA INC | zanubrutinib | 72579-011 |
>Company | >Ingredient | >NDC |
ZANUBRUTINIB drug variants not containing SODIUM LAURYL SULFATE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
Excipient focus: TITANIUM DIOXIDE
ZANUBRUTINIB drug variants containing TITANIUM DIOXIDE
Company | Ingredient | NDC |
---|---|---|
BEIGENE USA INC | zanubrutinib | 72579-011 |
>Company | >Ingredient | >NDC |
ZANUBRUTINIB drug variants not containing TITANIUM DIOXIDE
Company | Ingredient | NDC |
---|---|---|
>Company | >Ingredient | >NDC |
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