Tuesday, Sep 29, 2026

"us-food-drug-administration"

US FDA approves Granules India’s Abbreviated New Drug Application

Granules announced that US Food & Drug Administration (US FDA) has approved its ANDA for Venlafaxine Hydrochloride Extended-Release Capsules.
Granules gets FDA nod for capsules to treat low blood potassium

The capsules would be manufactured at the company's Hyderabad facility and are expected to be launched shortly, the filing said.

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