Scientific principles in design of drug dosage formulations.
- 8 January 1972
- Vol. 1 (5792) , 102-106
- https://doi.org/10.1136/bmj.1.5792.102
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Hazard of Therapeutic Nonequivalency of Drug Products*Journal of the American Pharmaceutical Association (1961), 1969
- Therapeutic Nonequivalence of Oxytetracycline CapsulesJAMA, 1969
- Physiochemical factors influencing the absorption of the anhydrous and trihydrate forms of ampicillin.1968
- Effect of polymorphism on the absorption of chloramphenicol from chloramphenicol palmitateJournal of Pharmaceutical Sciences, 1967
- Influence of the Absorption Rate of Tolbutamide on the Rate of Decline of Blood Sugar Levels in Normal HumansJournal of Pharmaceutical Sciences, 1962
- Loss of Sensitivity in Distinguishing Real Differences in Dissolution Rates Due to Increasing Intensity of AgitationJournal of Pharmaceutical Sciences, 1962
- Prediction of Stability in Pharmaceutical Preparations VIIIJournal of Pharmaceutical Sciences, 1962
- The effect of dosage form upon the gastrointestinal absorption rate of salicylates.1961
- Comparison of Dissolution and Absorption Rates of Different Commercial Aspirin TabletsJournal of Pharmaceutical Sciences, 1961
- Physiological Availability of Dicumarol.1960