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Alembic Pharma gets USFDA approval for Bupropion Hydrochloride tablets

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The drug approval is for strengths of 75 mg and 100 mg and is used to treat major depressive disorder

Alembic Pharmaceuticals has received USFDA approval for Bupropion Hydrochloride tablets, used for treatment of major depressive disorder. “The company has received approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Bupropion Hydrochloride tablets,” Alembic Pharmaceuticals said in a BSE filing.

The approval is for strengths of 75 mg and 100 mg. The approved product is therapeutically equivalent to the reference listed drug product (RLD) Wellbutrin tablets of GlaxoSmithKline.

Quoting IMS December 2017 data, the company said Bupropion Hydrochloride tablets had an estimated market size of $37 million.

The company now has a total of 72 ANDA approvals from the USFDA.

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