List of Excipients in API letrozole tablets

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Excipients in ANDA-approved (generic) drugs containing letrozole tablets

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Company	Ingredient	NDC	Excipient
Avet Pharmaceuticals Inc	letrozole tablets	23155-875	CELLULOSE, MICROCRYSTALLINE
Avet Pharmaceuticals Inc	letrozole tablets	23155-875	HYPROMELLOSE 2208
Avet Pharmaceuticals Inc	letrozole tablets	23155-875	LACTOSE MONOHYDRATE
Avet Pharmaceuticals Inc	letrozole tablets	23155-875	MAGNESIUM STEARATE
Avet Pharmaceuticals Inc	letrozole tablets	23155-875	SODIUM STARCH GLYCOLATE TYPE A
>Company	>Ingredient	>NDC	>Excipient

Detailed excipient profiles for letrozole tablets

Excipient focus: CELLULOSE, MICROCRYSTALLINE

letrozole tablets drug variants containing CELLULOSE, MICROCRYSTALLINE

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Company	Ingredient	NDC
Avet Pharmaceuticals Inc	letrozole tablets	23155-875
Upsher-Smith Laboratories LLC	letrozole tablets	24979-726
Golden State Medical Supply Inc	letrozole tablets	51407-986
Bryant Ranch Prepack	letrozole tablets	71335-2396
>Company	>Ingredient	>NDC

letrozole tablets drug variants not containing CELLULOSE, MICROCRYSTALLINE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: HYPROMELLOSE 2208

letrozole tablets drug variants containing HYPROMELLOSE 2208

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Company	Ingredient	NDC
Avet Pharmaceuticals Inc	letrozole tablets	23155-875
Bryant Ranch Prepack	letrozole tablets	71335-2396
>Company	>Ingredient	>NDC

letrozole tablets drug variants not containing HYPROMELLOSE 2208

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Company	Ingredient	NDC
Upsher-Smith Laboratories LLC	letrozole tablets	24979-726
Golden State Medical Supply Inc	letrozole tablets	51407-986
>Company	>Ingredient	>NDC

Excipient focus: LACTOSE MONOHYDRATE

letrozole tablets drug variants containing LACTOSE MONOHYDRATE

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Company	Ingredient	NDC
Avet Pharmaceuticals Inc	letrozole tablets	23155-875
Upsher-Smith Laboratories LLC	letrozole tablets	24979-726
Golden State Medical Supply Inc	letrozole tablets	51407-986
Bryant Ranch Prepack	letrozole tablets	71335-2396
>Company	>Ingredient	>NDC

letrozole tablets drug variants not containing LACTOSE MONOHYDRATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: MAGNESIUM STEARATE

letrozole tablets drug variants containing MAGNESIUM STEARATE

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Company	Ingredient	NDC
Avet Pharmaceuticals Inc	letrozole tablets	23155-875
Upsher-Smith Laboratories LLC	letrozole tablets	24979-726
Golden State Medical Supply Inc	letrozole tablets	51407-986
Bryant Ranch Prepack	letrozole tablets	71335-2396
>Company	>Ingredient	>NDC

letrozole tablets drug variants not containing MAGNESIUM STEARATE

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Company	Ingredient	NDC
>Company	>Ingredient	>NDC

Excipient focus: SILICON DIOXIDE

letrozole tablets drug variants containing SILICON DIOXIDE

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Company	Ingredient	NDC
Upsher-Smith Laboratories LLC	letrozole tablets	24979-726
Golden State Medical Supply Inc	letrozole tablets	51407-986
>Company	>Ingredient	>NDC

letrozole tablets drug variants not containing SILICON DIOXIDE

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Company	Ingredient	NDC
Avet Pharmaceuticals Inc	letrozole tablets	23155-875
Bryant Ranch Prepack	letrozole tablets	71335-2396
>Company	>Ingredient	>NDC

Excipient focus: SODIUM STARCH GLYCOLATE TYPE A

letrozole tablets drug variants containing SODIUM STARCH GLYCOLATE TYPE A

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Company	Ingredient	NDC
Avet Pharmaceuticals Inc	letrozole tablets	23155-875
Bryant Ranch Prepack	letrozole tablets	71335-2396
>Company	>Ingredient	>NDC

letrozole tablets drug variants not containing SODIUM STARCH GLYCOLATE TYPE A

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Company	Ingredient	NDC
Upsher-Smith Laboratories LLC	letrozole tablets	24979-726
Golden State Medical Supply Inc	letrozole tablets	51407-986
>Company	>Ingredient	>NDC

Excipient focus: SODIUM STARCH GLYCOLATE TYPE A POTATO

letrozole tablets drug variants containing SODIUM STARCH GLYCOLATE TYPE A POTATO

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Company	Ingredient	NDC
Upsher-Smith Laboratories LLC	letrozole tablets	24979-726
Golden State Medical Supply Inc	letrozole tablets	51407-986
>Company	>Ingredient	>NDC

letrozole tablets drug variants not containing SODIUM STARCH GLYCOLATE TYPE A POTATO

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Company	Ingredient	NDC
Avet Pharmaceuticals Inc	letrozole tablets	23155-875
Bryant Ranch Prepack	letrozole tablets	71335-2396
>Company	>Ingredient	>NDC

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