US Food and Drug Administration USFDA

US Food and Drug Administration (USFDA). 2002. Report to Congress. Reports on Postmarketing Studies [FDAMA 130], Washington, DC FDA. 

United States of America US Food and Drug Administration (USFDA) http //WWW.fda.gov/AnimalVeterinary/ GuidanceComplianceEnforcement/Guidance forIndustry/ucml23817.htm... 

USFDA (US Food and Drug Administration) (2001). Prescription drug products doxycycline and penicillin G procaine... 

Gad SC and Chengelis CP (1999) Acute Toxicology Principles and Methods, 2nd edn. San Diego, CA Academic Press. USFDA (2000) Redbook 2000. US Food and Drug Administration. 

The dissolution rate studies of carvedilol alone and its spherical agglomerates were performed in triplicate in a dissolution apparatus (Electrolab, India) using the paddle method (USP Type II). Dissolution studies were carried out using 900 ml of O.IN HCl (pH 1.2) at 37 0.5 OC at 50 rpm as per US FDA guidelines (U.S. Food and drug administration [USFDA], 2010 and Bhutani et al., 2007.). 12.5 mg of carvedilol or its equivalent amount of... 

US Code, 21CFR177.1630, USFDA Premarket Notifications for Food Contact Substances, United States Food and Drug Administration, Washington, DC, October 5, 2000. 

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