List of Excipients in API epoprostenol

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Excipients in NDA-approved (novel) drugs containing epoprostenol

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Company	Tradename	Ingredient	NDC	Excipient	Potential Generic Entry
Actelion Pharmaceuticals US Inc	VELETRI	epoprostenol	66215-403	ARGININE
Actelion Pharmaceuticals US Inc	VELETRI	epoprostenol	66215-403	SODIUM HYDROXIDE
Actelion Pharmaceuticals US Inc	VELETRI	epoprostenol	66215-403	SUCROSE
GlaxoSmithKline LLC	FLOLAN	epoprostenol sodium	0173-0517	GLYCINE
>Company	>Tradename	>Ingredient	>NDC	>Excipient	>Potential Generic Entry

Excipients in ANDA-approved (generic) drugs containing epoprostenol

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Company	Ingredient	NDC	Excipient
Sun Pharmaceutical Industries Inc	epoprostenol	62756-059	GLYCINE
Sun Pharmaceutical Industries Inc	epoprostenol	62756-059	SODIUM HYDROXIDE
Sun Pharmaceutical Industries Inc	epoprostenol	62756-059	SUCROSE
Mylan Institutional LLC	epoprostenol	67457-587	ARGININE
>Company	>Ingredient	>NDC	>Excipient

Detailed excipient profiles for epoprostenol

Excipient focus: ARGININE

epoprostenol drug variants containing ARGININE

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Company	Ingredient	NDC
Actelion Pharmaceuticals US Inc	epoprostenol	66215-403
Mylan Institutional LLC	epoprostenol	67457-587
>Company	>Ingredient	>NDC

epoprostenol drug variants not containing ARGININE

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Company	Ingredient	NDC
Sun Pharmaceutical Industries Inc	epoprostenol	62756-059
GlaxoSmithKline LLC	epoprostenol sodium	0173-0517
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985
>Company	>Ingredient	>NDC

Excipient focus: GLYCINE

epoprostenol drug variants containing GLYCINE

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Company	Ingredient	NDC
Sun Pharmaceutical Industries Inc	epoprostenol	62756-059
GlaxoSmithKline LLC	epoprostenol sodium	0173-0517
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985
>Company	>Ingredient	>NDC

epoprostenol drug variants not containing GLYCINE

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Company	Ingredient	NDC
Actelion Pharmaceuticals US Inc	epoprostenol	66215-403
Mylan Institutional LLC	epoprostenol	67457-587
>Company	>Ingredient	>NDC

Excipient focus: MANNITOL

epoprostenol 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 drug variants not containing MANNITOL

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Company	Ingredient	NDC
Sun Pharmaceutical Industries Inc	epoprostenol	62756-059
Actelion Pharmaceuticals US Inc	epoprostenol	66215-403
Mylan Institutional LLC	epoprostenol	67457-587
>Company	>Ingredient	>NDC

Excipient focus: SODIUM CHLORIDE

epoprostenol 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 drug variants not containing SODIUM CHLORIDE

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Company	Ingredient	NDC
Sun Pharmaceutical Industries Inc	epoprostenol	62756-059
Actelion Pharmaceuticals US Inc	epoprostenol	66215-403
Mylan Institutional LLC	epoprostenol	67457-587
>Company	>Ingredient	>NDC

Excipient focus: SODIUM HYDROXIDE

epoprostenol drug variants containing SODIUM HYDROXIDE

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Company	Ingredient	NDC
Sun Pharmaceutical Industries Inc	epoprostenol	62756-059
Actelion Pharmaceuticals US Inc	epoprostenol	66215-403
Mylan Institutional LLC	epoprostenol	67457-587
Teva Parenteral Medicines Inc	epoprostenol sodium	0703-1985
>Company	>Ingredient	>NDC

epoprostenol drug variants not containing SODIUM HYDROXIDE

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

Excipient focus: SUCROSE

epoprostenol drug variants containing SUCROSE

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Company	Ingredient	NDC
Sun Pharmaceutical Industries Inc	epoprostenol	62756-059
Actelion Pharmaceuticals US Inc	epoprostenol	66215-403
Mylan Institutional LLC	epoprostenol	67457-587
>Company	>Ingredient	>NDC

epoprostenol drug variants not containing SUCROSE

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

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