Guidance for industry : potassium chloride modified-release tablets and capsules, in vivo bioequivalence and in vitro dissolution testing.

Bibliographic Details
Corporate Author:	Center for Drug Evaluation and Research (U.S.). Office of Generic Drugs
Format:	Government Document eBook
Language:	English
Published:	Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2005]
Subjects:	Potassium chloride. Drugs > Therapeutic equivalency > Government policy > United States. Tablets (Medicine) > Testing > Government policy > United States. Capsules (Pharmacy) > Testing > Government policy > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS117081

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