Glenmark Generics Inc

Glenmark Pharmaceuticals on Monday said it has entered into an agreement with US-based Particle Sciences Inc to develop and market a generic version of Celgene's ABRAXANE, which is used in treatments of breast and lung cancers.

Glenmark Pharmaceuticals has received the final nod from the US health regulator for a generic version of anti-bacterial drug Zyvox. "Glenmark Pharmaceuticals Inc, USA, has been granted final approval by the US Food & Drug Administration (USFDA) for the Linezolid tablets, 600 mg," Glenmark Pharmaceuticals said in a statement.

It said in a statement that Glenmark Pharmaceuticals Inc, USA, a subsidiary of the company, has been granted tentative approval by the United States Food & Drug Administration (USFDA) for Calcipotriene cream, 0.005 per cent.

Pharmaceutical major Glenmark on Wednesday said its US subsidiary will pay $25 million to settle a pricing investigation there.

Glenmark Pharmaceuticals on Tuesday said it has received the final approval from the US Food and Drug Administration (FDA) for sale of drugs meant to prevent post-menopause osteoporosis.

Glenmark Pharmaceuticals on Thursday announced receipt of approval from the US Food and Drug Administration (FDA) to sell its generic version of AbbVie Inc's blood pressure drug Tarka in the American market.

Glenmark Generics Inc (GGI) has been granted the final abbreviated new drug approval (ANDA) from the United States Food and Drug Administration (USFDA) for Omeprazole Delayed Release Capsules, their generic version of Prilosec by AstraZeneca, a company statement said.

Glenmark Generics Inc USA, the subsidiary of Glenmark Generics Ltd, has been granted final approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Fluocinonide cream USP (0.1 per cent), Glenmark Pharmaceuticals said in a statement.

Glenmark Pharmaceuticals on Thursday posted a consolidated net profit of Rs 43.41 crore for the fourth quarter that ended on March 31, 2014.

Ranbaxy Laboratories Ltd has been hit by more regulatory scrutiny sparked by a US ban on the bulk of its drugs, in a backlash that could bump up compliance costs and erode profitability among some Indian makers of generic drugs.

The complaint has been filed against Glenmark trying to commercialise the product before the expiry of patent which is a generic version of Treanda, it added.

Glenmark Generics Inc USA, the subsidiary of Glenmark Generics Ltd has received nod for its Hydrocortisone Butyrate Cream USP (0.1 per cent), abbreviated new drug approval (ANDA) from the United States Food and Drug Administration (USFDA), Glenmark Pharmaceuticals said in a statement.

Glenmark Generics Inc, the US-based subsidiary of Glenmark Generics Ltd (GGL), has been granted final abbreviated new drug approval (ANDA) from the United States Food and Drug Administration (USFDA) for Acamprosate Calcium Delayed Release Tablets, Glenmark Pharma said in a statement.

Drug firm Glenmark Pharmaceuticals said it has received final approval from the US health regulator for its generic contraceptive norgestimate and ethinyl estradiol tablets.

Glenmark Pharmaceuticals on Wednesday said it has received final approval from the US health regulator for its generic Imiquimod cream used for treating skin disorders.

Glenmark Pharmaceuticals on Monday said it has entered into an agreement with US-based Particle Sciences Inc to develop and market a generic version of Celgene's ABRAXANE, which is used in treatments of breast and lung cancers.

Glenmark Pharmaceuticals has received the final nod from the US health regulator for a generic version of anti-bacterial drug Zyvox. "Glenmark Pharmaceuticals Inc, USA, has been granted final approval by the US Food & Drug Administration (USFDA) for the Linezolid tablets, 600 mg," Glenmark Pharmaceuticals said in a statement.

It said in a statement that Glenmark Pharmaceuticals Inc, USA, a subsidiary of the company, has been granted tentative approval by the United States Food & Drug Administration (USFDA) for Calcipotriene cream, 0.005 per cent.

Pharmaceutical major Glenmark on Wednesday said its US subsidiary will pay $25 million to settle a pricing investigation there.

Glenmark Pharmaceuticals on Tuesday said it has received the final approval from the US Food and Drug Administration (FDA) for sale of drugs meant to prevent post-menopause osteoporosis.

Glenmark Pharmaceuticals on Thursday announced receipt of approval from the US Food and Drug Administration (FDA) to sell its generic version of AbbVie Inc's blood pressure drug Tarka in the American market.

Glenmark Generics Inc (GGI) has been granted the final abbreviated new drug approval (ANDA) from the United States Food and Drug Administration (USFDA) for Omeprazole Delayed Release Capsules, their generic version of Prilosec by AstraZeneca, a company statement said.

Glenmark Generics Inc USA, the subsidiary of Glenmark Generics Ltd, has been granted final approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Fluocinonide cream USP (0.1 per cent), Glenmark Pharmaceuticals said in a statement.

Glenmark Pharmaceuticals on Thursday posted a consolidated net profit of Rs 43.41 crore for the fourth quarter that ended on March 31, 2014.

Ranbaxy Laboratories Ltd has been hit by more regulatory scrutiny sparked by a US ban on the bulk of its drugs, in a backlash that could bump up compliance costs and erode profitability among some Indian makers of generic drugs.

The complaint has been filed against Glenmark trying to commercialise the product before the expiry of patent which is a generic version of Treanda, it added.

Glenmark Generics Inc USA, the subsidiary of Glenmark Generics Ltd has received nod for its Hydrocortisone Butyrate Cream USP (0.1 per cent), abbreviated new drug approval (ANDA) from the United States Food and Drug Administration (USFDA), Glenmark Pharmaceuticals said in a statement.

Glenmark Generics Inc, the US-based subsidiary of Glenmark Generics Ltd (GGL), has been granted final abbreviated new drug approval (ANDA) from the United States Food and Drug Administration (USFDA) for Acamprosate Calcium Delayed Release Tablets, Glenmark Pharma said in a statement.

Drug firm Glenmark Pharmaceuticals said it has received final approval from the US health regulator for its generic contraceptive norgestimate and ethinyl estradiol tablets.

Glenmark Pharmaceuticals on Wednesday said it has received final approval from the US health regulator for its generic Imiquimod cream used for treating skin disorders.