Cetirizine Hydrochloride Tablets (OTC) ANDA Are Approved
It is reported that the U.S. Food and Drug Administration (FDA) ratified Abbreviated New Drug Application (ANDA) for Cetirizine hydrochloride tablets (OTC). The company that received approval from FDA and intends to market allergy pills is Taro Pharmaceutical Industries Ltd. In fact, Taro is a multinational, science-based pharmaceutical company, using methods of discovery and development in manufacturing. More, the company is known for marketing of the highest quality medicines.
Zyrtec (Cetirizine) Tablets are related to nonprescription allergy meds used for the temporary relief of symptoms caused by hay fever or other respiratory allergies in adults and children from 2 years; also for the relief of itching because of hives in children from 6 years and adults. Generic Cetirizine is a well-known allergy medicine, annual sales of what are approximately $350 million in the U.S.
Actually, Taro’s Cetirizine Tablets (Cetirizine 10mg and Cetirizine 5mg) are bioequivalent to Zyrtec Hives Relief Tablets and McNeil Consumer Healthcare’s Zyrtec Allergy Tablets.
