Pharmacopeial standards and specifications for bulk drugs and solid oral dosage forms. Similarities and differences
- 1 December 1967
- journal article
- research article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 56 (12), 1622-1641
- https://doi.org/10.1002/jps.2600561218
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Variability of Uniformity of Weight Test as an Indicator of the Amount of Active Ingredient in TabletsJournal of Pharmaceutical Sciences, 1967
- Experiences with Unit-to-Unit Variations in TabletsJournal of Pharmaceutical Sciences, 1964
- Dosage Variation in Compressed TabletsJournal of Pharmaceutical Sciences, 1963
- Dosage Variation in TabletsJournal of Pharmaceutical Sciences, 1963
- Acceptance Sampling of Finished Pharmaceutical ProductsJournal of Pharmaceutical Sciences, 1962
- Selection, Evaluation, and Control of the Assay of the Pharmaceutical Product IIJournal of Pharmaceutical Sciences, 1962
- Selection, Evaluation, and Control of the Assay of the Pharmaceutical Product IJournal of Pharmaceutical Sciences, 1962
- Uniformity of Drug Dosage in Compressed TabletsJournal of Pharmaceutical Sciences, 1961
- Mixing of Pharmaceutical Solids: The General Approach * *Received August 21, 1959, from the School of Pharmacy, University of London, England.Journal of the American Pharmaceutical Association (Scientific ed.), 1960
- The Uniformity of Distribution of Phosphorus Compounds in Tablet Matrices Using Radioactive Tracer Techniques**School of Pharmacy, Purdue University, Lafayette, Ind.Journal of the American Pharmaceutical Association (Scientific ed.), 1958