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Last Updated: December 22, 2024

List of Excipients in API epoprostenol sodium

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Excipients in NDA-approved (novel) drugs containing epoprostenol sodium

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Company	Tradename	Ingredient	NDC	Excipient	Potential Generic Entry
GlaxoSmithKline LLC	FLOLAN	epoprostenol sodium	0173-0517	GLYCINE
GlaxoSmithKline LLC	FLOLAN	epoprostenol sodium	0173-0517	MANNITOL
GlaxoSmithKline LLC	FLOLAN	epoprostenol sodium	0173-0517	SODIUM CHLORIDE
>Company	>Tradename	>Ingredient	>NDC	>Excipient	>Potential Generic Entry

Excipients in ANDA-approved (generic) drugs containing epoprostenol sodium

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Company	Ingredient	NDC	Excipient
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985	GLYCINE
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985	MANNITOL
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985	SODIUM CHLORIDE
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985	SODIUM HYDROXIDE
>Company	>Ingredient	>NDC	>Excipient

Detailed excipient profiles for epoprostenol sodium

Excipient focus: GLYCINE

epoprostenol sodium drug variants containing GLYCINE

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Company	Ingredient	NDC
GlaxoSmithKline LLC	epoprostenol sodium	0173-0517
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985
>Company	>Ingredient	>NDC

epoprostenol sodium drug variants not containing GLYCINE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: MANNITOL

epoprostenol sodium drug variants containing MANNITOL

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Company	Ingredient	NDC
GlaxoSmithKline LLC	epoprostenol sodium	0173-0517
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985
>Company	>Ingredient	>NDC

epoprostenol sodium drug variants not containing MANNITOL

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM CHLORIDE

epoprostenol sodium drug variants containing SODIUM CHLORIDE

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Company	Ingredient	NDC
GlaxoSmithKline LLC	epoprostenol sodium	0173-0517
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985
>Company	>Ingredient	>NDC

epoprostenol sodium drug variants not containing SODIUM CHLORIDE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM HYDROXIDE

epoprostenol sodium drug variants containing SODIUM HYDROXIDE

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Company	Ingredient	NDC
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985
>Company	>Ingredient	>NDC

epoprostenol sodium drug variants not containing SODIUM HYDROXIDE

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Company	Ingredient	NDC
GlaxoSmithKline LLC	epoprostenol sodium	0173-0517
>Company	>Ingredient	>NDC

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