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FDA approval activities for this prescription drug:

Cozaar (losartan potassium) Tablets, Merck & Co., NDA 20-386/S032 3/25/03 4/1/03 4/1/03 7/8/03 Cozaar (losartan potassium) Tablets, 25, 50, & 100 mg, Merck & Co., NDA 20-386/S028 9/17/02 9/20/02 9/17/02 2/4/03 Cozaar (losartan potassium) Tablets, 25, 50, & 100 mg; Hyzaar (losartan potassium / hydrochlorothiazide) Tablets, 50-12.5 & 100-25 Merck & Co., NDA 20-386/S020 & 20-387/S017 1/19/00 6/6/01 Cozaar (losartan potassium) Tablets, 25, 50, & 100 mg; Hyzaar (losartan potassium / hydrochlorothiazide) Tablets, 50-12.5 & 100-25 Merck & Co., NDA 20-386/S018 & 20-387/S014 1/28/00 6/6/01 Cozaar (losartan potassium) Tablets, 25 & 50 mg Merck Research NDA 20-386/S-015 11/24/98 3/13/00 Cozaar (losartan potassium) Tablets, 25 & 50 mg Merck Research NDA 20-386/S-008 10/13/98 9/14/01 Cozaar (losartan potassium) Tablets, 25 & 50 mg Merck & Co. NDA 20-386/S-017 Hyzaar (losartan potassium/hydrochlorothiazide), Merck & Co., NDA 20-387/S-013 & S-015 & S-027 9/30/03 10/10/03 10/10/03 Hyzaar (losartan potassium/hydrochlorothiazide) Tablets, 50/12.5 and 100/25 mg. Merck & Co., NDA 20-387/S-024 11/7/02 11/18/02 Hyzaar (losartan potassium/hydrochlorothiazide) Tablets, 50-12.5 mg Merck Research NDA 20-387/S6 8/24/98 12/3/01 Hyzaar (losartan potassium/hydrochlorothiazide) Tablets, 50-12.5 mg Merck Research NDA 20-387/S8 11/10/98 12/3/01 Hyzaar 50-12.5 (losartan potassium/hydrochlorothiazide) Tablets, 50-12.5 mg Merck Research NDA 20-387/S10 8/25/98 12/3/01 Hyzaar 50 (losartan potassium/hydrochlorothiazide) Tablets, 50-12.5 mg Merck Research NDA 20-387/S-011 11/24/98 3/13/00 Hyzaar 50 (losartan potassium/hydrochlorothiazide) Tablets, 50-12.5 mg & 100-25 mg Merck Research NDA 20-387/S-012

For the latest approval information, please locate this API using this index.

 
                                                                                  


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