List of Excipients in API DIAZOXIDE

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Excipients in NDA-approved (novel) drugs containing DIAZOXIDE

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Company	Tradename	Ingredient	NDC	Excipient	Potential Generic Entry
Teva Pharmaceuticals USA Inc	PROGLYCEM	diazoxide	0575-6200	ALCOHOL
Teva Pharmaceuticals USA Inc	PROGLYCEM	diazoxide	0575-6200	CARBOXYMETHYLCELLULOSE SODIUM
Teva Pharmaceuticals USA Inc	PROGLYCEM	diazoxide	0575-6200	HYDROCHLORIC ACID
Teva Pharmaceuticals USA Inc	PROGLYCEM	diazoxide	0575-6200	MAGNESIUM ALUMINUM SILICATE
Teva Pharmaceuticals USA Inc	PROGLYCEM	diazoxide	0575-6200	METHYLPARABEN
>Company	>Tradename	>Ingredient	>NDC	>Excipient	>Potential Generic Entry

Excipients in ANDA-approved (generic) drugs containing DIAZOXIDE

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Company	Ingredient	NDC	Excipient
Par Pharmaceutical Inc	diazoxide	0254-1010	ALCOHOL
Par Pharmaceutical Inc	diazoxide	0254-1010	CARBOXYMETHYLCELLULOSE SODIUM
Par Pharmaceutical Inc	diazoxide	0254-1010	FD&C RED NO. 40
Par Pharmaceutical Inc	diazoxide	0254-1010	FD&C YELLOW NO. 6
Par Pharmaceutical Inc	diazoxide	0254-1010	HYDROCHLORIC ACID
>Company	>Ingredient	>NDC	>Excipient

Detailed excipient profiles for DIAZOXIDE

Excipient focus: ALCOHOL

DIAZOXIDE drug variants containing ALCOHOL

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing ALCOHOL

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: CARBOXYMETHYLCELLULOSE SODIUM

DIAZOXIDE drug variants containing CARBOXYMETHYLCELLULOSE SODIUM

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing CARBOXYMETHYLCELLULOSE SODIUM

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: FD&C RED NO. 40

DIAZOXIDE drug variants containing FD&C RED NO. 40

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing FD&C RED NO. 40

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Company	Ingredient	NDC
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

Excipient focus: FD&C YELLOW NO. 6

DIAZOXIDE drug variants containing FD&C YELLOW NO. 6

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing FD&C YELLOW NO. 6

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Company	Ingredient	NDC
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

Excipient focus: HYDROCHLORIC ACID

DIAZOXIDE drug variants containing HYDROCHLORIC ACID

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing HYDROCHLORIC ACID

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: MAGNESIUM ALUMINUM SILICATE

DIAZOXIDE drug variants containing MAGNESIUM ALUMINUM SILICATE

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing MAGNESIUM ALUMINUM SILICATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: METHYLPARABEN

DIAZOXIDE drug variants containing METHYLPARABEN

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing METHYLPARABEN

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: POLOXAMER 188

DIAZOXIDE drug variants containing POLOXAMER 188

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing POLOXAMER 188

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Company	Ingredient	NDC
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

Excipient focus: PROPYLENE GLYCOL

DIAZOXIDE drug variants containing PROPYLENE GLYCOL

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing PROPYLENE GLYCOL

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: PROPYLENE OXIDE

DIAZOXIDE drug variants containing PROPYLENE OXIDE

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Company	Ingredient	NDC
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing PROPYLENE OXIDE

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
>Company	>Ingredient	>NDC

Excipient focus: PROPYLPARABEN

DIAZOXIDE drug variants containing PROPYLPARABEN

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing PROPYLPARABEN

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM BENZOATE

DIAZOXIDE drug variants containing SODIUM BENZOATE

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing SODIUM BENZOATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM HYDROXIDE

DIAZOXIDE drug variants containing SODIUM HYDROXIDE

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Company	Ingredient	NDC
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing SODIUM HYDROXIDE

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

Excipient focus: SORBITOL

DIAZOXIDE drug variants containing SORBITOL

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing SORBITOL

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Company	Ingredient	NDC
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

Excipient focus: SORBITOL SOLUTION 70%

DIAZOXIDE drug variants containing SORBITOL SOLUTION 70%

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Company	Ingredient	NDC
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing SORBITOL SOLUTION 70%

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
>Company	>Ingredient	>NDC

Excipient focus: WATER

DIAZOXIDE drug variants containing WATER

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Company	Ingredient	NDC
Par Pharmaceutical Inc	diazoxide	0254-1010
Teva Pharmaceuticals USA Inc	diazoxide	0575-6200
e5 Pharma LLC	diazoxide	13517-100
>Company	>Ingredient	>NDC

DIAZOXIDE drug variants not containing WATER

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Company	Ingredient	NDC
TriRx Huntsville Pharmaceutical Services LLC	diazoxide oral suspension	80432-057
>Company	>Ingredient	>NDC

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