Mylan

Mylan Distributes Free EpiPens to U.S. Schools

Distribution of the medical devices is intended to prevent students from suffering life-threatening allergic reactions at school.

Since Mylan Specialty L.P., the fully-integrated specialty pharmaceutical business of Mylan Inc. (Nasdaq: MYL), launched the EpiPen4Schools program in August 2012, thousands of schools across the country have elected to participate and redeem free EpiPen® or EpiPen Jr® (epinephrine) Auto-Injectors. The program was created to help schools have improved access to epinephrine in the event a person experiences a life-threatening allergic reaction (anaphylaxis) at school.

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Mylan Distributes Free EpiPens to U.S. Schools

Distribution of the medical devices is intended to prevent students from suffering life-threatening allergic reactions at school.

Since Mylan Specialty L.P., the fully-integrated specialty pharmaceutical business of Mylan Inc. (Nasdaq: MYL), launched the EpiPen4Schools program in August 2012, thousands of schools across the country have elected to participate and redeem free EpiPen® or EpiPen Jr® (epinephrine) Auto-Injectors. The program was created to help schools have improved access to epinephrine in the event a person experiences a life-threatening allergic reaction (anaphylaxis) at school.

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Mylan Launches Generic Maxalt MLT Tablets

The pharmaceutical firm has received FDA approval for its migraine treatment.

Mylan Inc. today announced that its subsidiary Mylan Pharmaceuticals has received final approval from the U.S. Food and Drug Administration (FDA) for its Abbreviated New Drug Applications (ANDA) for Rizatriptan Benzoate Orally Disintegrating Tablets, 5 mg (base) and 10 mg (base), and Rizatriptan Benzoate Tablets, 5 mg (base) and 10 mg (base). These products are the generic versions of Merck's Maxalt MLT® Tablets and Maxalt® Tablets, respectively, and are indicated for the acute treatment of migraine with or without aura in adults.

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Mylan Launches Generic Version of Atacand HCT

The company has attained 180 days of marketing exclusivity on the 32/25 mg strength of the hypertension treatment.

Mylan Inc. today announced that its subsidiary Mylan Pharmaceuticals Inc. has received final approval from the U.S. Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for Candesartan Cilexetil and Hydrochlorothiazide Tablets, 16/12.5 mg, 32/12.5 mg and 32/25 mg. This product is the generic version of AstraZeneca's Atacand HCT, and is indicated for the treatment of hypertension. This fixed dose combination is not indicated for initial therapy.

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