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| FDA approval activities
for this prescription drug:
Midamor (amiloride HCl) & (amiloride HCL/ hydrochlorothiazide) Tablets, 5 & 5/50 mg respectively, Merck & Co., NDA 18-200/S-26 & 18-201/S-40 2/25/03 3/10/03 Midamor (amiloride hydrochloride) 5 mg Tablets and Moduretic (amiloride hydrochloride and hydrochlorothiazide) 5/50 mg Tablets, Merck & Co., NDA 18-200/S-024 & 18-201/S-037 AMILORIDE HYDROCHLORIDE Tablet; 5MG MIDAMOR MERCK 070346 AMILORIDE HYDROCHLORIDE Tablet; 5MG AMILORIDE HCL PAR 071111 AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Tablet; 5MG ANHYDROUS;50MG AMILORIDE HCL AND HYDROCHLOROTHIAZIDE BARR 073357 AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Tablet; 5MG ANHYDROUS;50MG AMILORIDE HCL AND HYDROCHLOROTHIAZIDE GENEVA 018201 AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Tablet; 5MG ANHYDROUS;50MG MODURETIC 5-50 MERCK 073209 AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Tablet; 5MG ANHYDROUS;50MG AMILORIDE HCL AND HYDROCHLOROTHIAZIDE MYLAN 070347 AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Tablet; 5MG ANHYDROUS;50MG HYDRO-RIDE PAR 070795 AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Tablet; 5MG ANHYDROUS;50MG AMILORIDE HCL AND HYDROCHLOROTHIAZIDE TEVA 073334 AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE Tablet; 5MG ANHYDROUS;50MG AMILORIDE HCL AND HYDROCHLOROTHIAZIDE WATSON |
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