FDA Drug Application (011722) for TENUATE by ACTAVIS LABS UT INC

Back to FDA Applications sponsored by ACTAVIS LABS UT INC

Application Number011722
Product Number002
FormTABLET;ORAL
Dosage25MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AA Products in conventional dosage forms not presenting bioequivalence problems
Reference Drug
Drug NameTENUATE
Active IngredientDIETHYLPROPION HYDROCHLORIDE



Back to FDA Applications sponsored by ACTAVIS LABS UT INC

Problems, Comments, Suggestions? Click here to contact Greg Thatcher

Please read my Disclaimer





Copyright (c) 2013 Thatcher Development Software, LLC. All rights reserved. No claim to original U.S. Gov't works.