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Corporate - Regulatory Bodies & Rulings
Ipca-Ranbaxy drug gets US nod

Our Bureau,

New Delhi, July 25 The less than a year old Ipca Laboratories and Ranbaxy Pharmaceuticals alliance has received its fourth US Food and Drugs Administration approval for three strengths of hydrochlorothiazide tablets.

The drugs will be manufactured initially at Ohm Laboratories, Ranbaxy’s Princeton-based facility, and marketed in the US healthcare system using the Ipca’s DMF approved active pharmaceutical ingredient (API) — hydrochlorothiazide.

The formulation is used as an adjunct therapy oedema, and the company claims the total annual market sales for the tablets in the US were $30.8 million during the last financial year.

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