Lupin recalls 4,113 cartons of oral contraceptive medicine in US market

Lupin is recalling 4,113 cartons of generic oral contraceptive tablets in the US due to manufacturing issues.

As per the latest enforcement report issued by the US Food and Drug Administration (FDA), Lupin’s US-based unit is recalling 4,113 cartons of Tydemy (drospirenone, ethinyl estradiol and levomefolate calcium tablets, 3 mg/0.03 mg/0.451 mg and levomefolate calcium tablets, 0.451 mg).

The affected lot has been produced at the company’s Pithampur-based manufacturing facility in Madhya Pradesh and distributed in the US by Baltimore-based Lupin Pharmaceuticals, Inc.

The company is recalling the lot due to it being “Subpotent Drug,” the US health regulator noted in the report.

Lupin initiated the nationwide recall on 19th November this year, it added.

The US FDA has classified both the recalls as class-III.

Last month, the US FDA had stated that the Mumbai-based drugmaker is recalling 16,272 bottles of Gatifloxacin Ophthalmic solution, an antibiotic used to treat bacterial infections of the eyes, in the US market.

As per the US health regulator, the company’s US-based unit is recalling the affected lot due to “failed stability specifications: Out-of-specification results observed in a water loss test that might affect the assay content and alter drug concentration.”