Alembic Pharma gets USFDA nod for Parkinson's disease treatment drugs

The company has received approval from the USFDA for its abbreviated new drug application Carbidopa and Levodopa extended-release tablets

alembic pharma
Press Trust of India New Delhi
1 min read Last Updated : Jun 06 2019 | 1:20 PM IST

Alembic Pharmaceuticals on Thursday said it has received approval from the US health regulator for Carbidopa and Levodopa extended-release tablets, used for treatment of Parkinson's disease.

The approved products are therapeutically equivalent to the reference listed drug Sinemet CR tablets of Merck Sharp & Dohme Corp.

The company has received approval from the US Food and Drug Administration (USFDA) for its abbreviated new drug application Carbidopa and Levodopa extended-release tablets in the strengths of 2.5 mg/100 mg and 50mg/200 mg, Alembic said in a BSE filing.

Quoting IQVIA sales data, the company said the two products had an estimated market size of $24 million for 12 months ended December 2018.

The company said it now has a total of 94 abbreviated new drug application (ANDA) approvals from the USFDA.

Shares of Alembic Pharmaceuticals were trading at Rs 511.05 apiece, down 0.08 per cent, on the BSE.

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First Published: Jun 06 2019 | 12:20 PM IST

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