Search results
dosage forms. Determine the type of units under test from the labeling and from observation, and apply the appropriate procedure to 6 or more dosage units.F For the purposes of this test, disintegration does not imply complete solution of the unit or even of its acti.
This test is provided to determine whether tablets, capsules, or granules USP 1-Aug-2019 disintegrate within the prescribed time when placed in a liquid medium at the experimental conditions presented below.
294 〈701〉 Disintegration / Physical Tests USP 35 Figure 1. Disintegration apparatus. (All dimensions are expressed in mm.) ate the apparatus, using water or the specified medium as Buccal Tablets—Apply the test for Uncoated Tablets. After the immersion fluid, maintained at 37±2°.
This test is provided to determine whether tablets or capsules disintegrate within the prescribed time when placed in a liquid medium under the experimental conditions presented below. For the purposes of this test, disintegration does not imply complete dissolution of the unit or even of its active constituent.
Dissolution testing as described in this chapter is a quality-con-made of a suitable, transparent plastic material having a specific trol tool to enable the performance of dietary supplements to begravity of between 1.18 and 1.20.
The USP Dissolution Methods Database contains the test conditions (except Tolerances or Acceptance Criteria) as stated in the sections referring to dissolution, disintegration, or drug release tests in the respective USP drug product monograph.
This test is provided to determine compliance with the dissolution requirements with a hemispherical bottom and with one of the following where stated in the individual
