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Last Updated: November 22, 2024

List of Excipients in API ZANUBRUTINIB

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Excipients in NDA-approved (novel) drugs containing ZANUBRUTINIB

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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
BEIGENE USA INC	BRUKINSA	zanubrutinib	72579-011	GELATIN	2037-08-15
BEIGENE USA INC	BRUKINSA	zanubrutinib	72579-011	MAGNESIUM STEARATE	2037-08-15
BEIGENE USA INC	BRUKINSA	zanubrutinib	72579-011	SILICON DIOXIDE	2037-08-15
BEIGENE USA INC	BRUKINSA	zanubrutinib	72579-011	SODIUM LAURYL SULFATE	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

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Company	Ingredient	NDC
BEIGENE USA INC	zanubrutinib	72579-011
>Company	>Ingredient	>NDC

ZANUBRUTINIB drug variants not containing CELLULOSE, MICROCRYSTALLINE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: CROSCARMELLOSE SODIUM

ZANUBRUTINIB drug variants containing CROSCARMELLOSE SODIUM

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Company	Ingredient	NDC
BEIGENE USA INC	zanubrutinib	72579-011
>Company	>Ingredient	>NDC

ZANUBRUTINIB drug variants not containing CROSCARMELLOSE SODIUM

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: FERROSOFERRIC OXIDE

ZANUBRUTINIB drug variants containing FERROSOFERRIC OXIDE

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Company	Ingredient	NDC
BEIGENE USA INC	zanubrutinib	72579-011
>Company	>Ingredient	>NDC

ZANUBRUTINIB drug variants not containing FERROSOFERRIC OXIDE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: GELATIN

ZANUBRUTINIB drug variants containing GELATIN

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Company	Ingredient	NDC
BEIGENE USA INC	zanubrutinib	72579-011
>Company	>Ingredient	>NDC

ZANUBRUTINIB drug variants not containing GELATIN

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: MAGNESIUM STEARATE

ZANUBRUTINIB drug variants containing MAGNESIUM STEARATE

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Company	Ingredient	NDC
BEIGENE USA INC	zanubrutinib	72579-011
>Company	>Ingredient	>NDC

ZANUBRUTINIB drug variants not containing MAGNESIUM STEARATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SILICON DIOXIDE

ZANUBRUTINIB drug variants containing SILICON DIOXIDE

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Company	Ingredient	NDC
BEIGENE USA INC	zanubrutinib	72579-011
>Company	>Ingredient	>NDC

ZANUBRUTINIB drug variants not containing SILICON DIOXIDE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM LAURYL SULFATE

ZANUBRUTINIB drug variants containing SODIUM LAURYL SULFATE

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Company	Ingredient	NDC
BEIGENE USA INC	zanubrutinib	72579-011
>Company	>Ingredient	>NDC

ZANUBRUTINIB drug variants not containing SODIUM LAURYL SULFATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: TITANIUM DIOXIDE

ZANUBRUTINIB drug variants containing TITANIUM DIOXIDE

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Company	Ingredient	NDC
BEIGENE USA INC	zanubrutinib	72579-011
>Company	>Ingredient	>NDC

ZANUBRUTINIB drug variants not containing TITANIUM DIOXIDE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

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