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Last Updated: November 5, 2024

List of Excipients in API fexofenadine hydrochloride oral

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Excipients in ANDA-approved (generic) drugs containing fexofenadine hydrochloride oral

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Company	Ingredient	NDC	Excipient
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426	EDETATE DISODIUM
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426	ETHYLPARABEN
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426	METHYLPARABEN
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426	MODIFIED CORN STARCH
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426	POLOXAMER 407
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426	PROPYLENE GLYCOL
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426	SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
>Company	>Ingredient	>NDC	>Excipient

Detailed excipient profiles for fexofenadine hydrochloride oral

Excipient focus: EDETATE DISODIUM

fexofenadine hydrochloride oral drug variants containing EDETATE DISODIUM

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing EDETATE DISODIUM

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: ETHYLPARABEN

fexofenadine hydrochloride oral drug variants containing ETHYLPARABEN

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing ETHYLPARABEN

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: METHYLPARABEN

fexofenadine hydrochloride oral drug variants containing METHYLPARABEN

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing METHYLPARABEN

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: MODIFIED CORN STARCH

fexofenadine hydrochloride oral drug variants containing MODIFIED CORN STARCH

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing MODIFIED CORN STARCH

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: POLOXAMER 407

fexofenadine hydrochloride oral drug variants containing POLOXAMER 407

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing POLOXAMER 407

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: PROPYLENE GLYCOL

fexofenadine hydrochloride oral drug variants containing PROPYLENE GLYCOL

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing PROPYLENE GLYCOL

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM PHOSPHATE, DIBASIC, ANHYDROUS

fexofenadine hydrochloride oral drug variants containing SODIUM PHOSPHATE, DIBASIC, ANHYDROUS

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing SODIUM PHOSPHATE, DIBASIC, ANHYDROUS

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

fexofenadine hydrochloride oral drug variants containing SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: STRAWBERRY

fexofenadine hydrochloride oral drug variants containing STRAWBERRY

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing STRAWBERRY

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SUCROSE

fexofenadine hydrochloride oral drug variants containing SUCROSE

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing SUCROSE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: TITANIUM DIOXIDE

fexofenadine hydrochloride oral drug variants containing TITANIUM DIOXIDE

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing TITANIUM DIOXIDE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: TRIACETIN

fexofenadine hydrochloride oral drug variants containing TRIACETIN

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing TRIACETIN

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: WATER

fexofenadine hydrochloride oral drug variants containing WATER

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing WATER

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: XANTHAN GUM

fexofenadine hydrochloride oral drug variants containing XANTHAN GUM

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing XANTHAN GUM

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: XYLITOL

fexofenadine hydrochloride oral drug variants containing XYLITOL

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Company	Ingredient	NDC
Aurohealth LLC	fexofenadine hydrochloride oral	58602-426
>Company	>Ingredient	>NDC

fexofenadine hydrochloride oral drug variants not containing XYLITOL

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>Company	>Ingredient	>NDC

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