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Last Updated: December 23, 2024

List of Excipients in API ubrogepant

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Excipients in NDA-approved (novel) drugs containing ubrogepant

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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
Allergan Inc	UBRELVY	ubrogepant	0023-6498	SODIUM STEARYL FUMARATE	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

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Company	Ingredient	NDC
Allergan Inc	ubrogepant	0023-6498
>Company	>Ingredient	>NDC

ubrogepant drug variants not containing CELLULOSE, MICROCRYSTALLINE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: COPOVIDONE K25-31

ubrogepant drug variants containing COPOVIDONE K25-31

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Company	Ingredient	NDC
Allergan Inc	ubrogepant	0023-6498
>Company	>Ingredient	>NDC

ubrogepant drug variants not containing COPOVIDONE K25-31

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: CROSCARMELLOSE SODIUM

ubrogepant drug variants containing CROSCARMELLOSE SODIUM

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Company	Ingredient	NDC
Allergan Inc	ubrogepant	0023-6498
>Company	>Ingredient	>NDC

ubrogepant drug variants not containing CROSCARMELLOSE SODIUM

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: MANNITOL

ubrogepant drug variants containing MANNITOL

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Company	Ingredient	NDC
Allergan Inc	ubrogepant	0023-6498
>Company	>Ingredient	>NDC

ubrogepant drug variants not containing MANNITOL

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SILICON DIOXIDE

ubrogepant drug variants containing SILICON DIOXIDE

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Company	Ingredient	NDC
Allergan Inc	ubrogepant	0023-6498
>Company	>Ingredient	>NDC

ubrogepant drug variants not containing SILICON DIOXIDE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM CHLORIDE

ubrogepant drug variants containing SODIUM CHLORIDE

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Company	Ingredient	NDC
Allergan Inc	ubrogepant	0023-6498
>Company	>Ingredient	>NDC

ubrogepant drug variants not containing SODIUM CHLORIDE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM STEARYL FUMARATE

ubrogepant drug variants containing SODIUM STEARYL FUMARATE

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Company	Ingredient	NDC
Allergan Inc	ubrogepant	0023-6498
>Company	>Ingredient	>NDC

ubrogepant drug variants not containing SODIUM STEARYL FUMARATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: VITAMIN E POLYETHYLENE GLYCOL SUCCINATE

ubrogepant drug variants containing VITAMIN E POLYETHYLENE GLYCOL SUCCINATE

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Company	Ingredient	NDC
Allergan Inc	ubrogepant	0023-6498
>Company	>Ingredient	>NDC

ubrogepant drug variants not containing VITAMIN E POLYETHYLENE GLYCOL SUCCINATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

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