www.fdanews.com/articles/91738-fda-approves-teva-s-generic-uniretic
FDA APPROVES TEVA'S GENERIC UNIRETIC
March 12, 2007
Teva Pharmaceutical Industries announced that the FDA has approved its abbreviated new drug application for moexipril HCl/hydrochlorothiazide tablets, 7.5 mg/12.5 mg, 15 mg/12.5 mg and 15 mg/25 mg. The company said it would begin shipping the products immediately.
The drug is the first AB-rated generic equivalent of Schwarz Pharma's Uniretic, which is indicated for the treatment of hypertension, Teva said.
The brand product has annual sales of approximately $30 million in the U.S., according to Teva.