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Last Updated: November 24, 2024

List of Excipients in API ponatinib hydrochloride

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Excipients in NDA-approved (novel) drugs containing ponatinib hydrochloride

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Company	Tradename	Ingredient	NDC	Excipient	Potential Generic Entry
Takeda Pharmaceuticals America Inc	ICLUSIG	ponatinib hydrochloride	63020-535	CELLULOSE, MICROCRYSTALLINE
Takeda Pharmaceuticals America Inc	ICLUSIG	ponatinib hydrochloride	63020-535	LACTOSE MONOHYDRATE
Takeda Pharmaceuticals America Inc	ICLUSIG	ponatinib hydrochloride	63020-535	MAGNESIUM STEARATE
Takeda Pharmaceuticals America Inc	ICLUSIG	ponatinib hydrochloride	63020-535	SILICON DIOXIDE
Takeda Pharmaceuticals America Inc	ICLUSIG	ponatinib hydrochloride	63020-535	SODIUM STARCH GLYCOLATE TYPE B POTATO
>Company	>Tradename	>Ingredient	>NDC	>Excipient	>Potential Generic Entry

Detailed excipient profiles for ponatinib hydrochloride

Excipient focus: CELLULOSE, MICROCRYSTALLINE

ponatinib hydrochloride drug variants containing CELLULOSE, MICROCRYSTALLINE

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Company	Ingredient	NDC
Takeda Pharmaceuticals America Inc	ponatinib hydrochloride	63020-535
>Company	>Ingredient	>NDC

ponatinib hydrochloride drug variants not containing CELLULOSE, MICROCRYSTALLINE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: LACTOSE MONOHYDRATE

ponatinib hydrochloride drug variants containing LACTOSE MONOHYDRATE

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Company	Ingredient	NDC
Takeda Pharmaceuticals America Inc	ponatinib hydrochloride	63020-535
>Company	>Ingredient	>NDC

ponatinib hydrochloride drug variants not containing LACTOSE MONOHYDRATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: MAGNESIUM STEARATE

ponatinib hydrochloride drug variants containing MAGNESIUM STEARATE

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Company	Ingredient	NDC
Takeda Pharmaceuticals America Inc	ponatinib hydrochloride	63020-535
>Company	>Ingredient	>NDC

ponatinib hydrochloride drug variants not containing MAGNESIUM STEARATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SILICON DIOXIDE

ponatinib hydrochloride drug variants containing SILICON DIOXIDE

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Company	Ingredient	NDC
Takeda Pharmaceuticals America Inc	ponatinib hydrochloride	63020-535
>Company	>Ingredient	>NDC

ponatinib hydrochloride drug variants not containing SILICON DIOXIDE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM STARCH GLYCOLATE TYPE B POTATO

ponatinib hydrochloride drug variants containing SODIUM STARCH GLYCOLATE TYPE B POTATO

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Company	Ingredient	NDC
Takeda Pharmaceuticals America Inc	ponatinib hydrochloride	63020-535
>Company	>Ingredient	>NDC

ponatinib hydrochloride drug variants not containing SODIUM STARCH GLYCOLATE TYPE B POTATO

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

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