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Free format text: Effective date: The present invention relates to the micronizing technology for insoluble polycrystal medicine Iguratimod, and the micronized Iguratimod has new crystallization and powder size of microns. The orally taken quick release preparation with micronized Iguratimod as active component, high efficiency disintegrant, surfactant, diluent, etc has obviously improved in vitro leaching rate and neec vivo I need a quick oral releae rate, and obviously raised bioavailability.

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Pharmaceutical composition prepared with micronized prasterone or sodium prasterone sulfate and use thereof. CNA en.

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Fast- and slow-release tablets for oral administration of flavonoids: rutin and quercetin.

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The Food and Drug Administration (FDA) is announcing the availability of a guidance for industry entitled ``Dissolution Testing of Immediate Release Solid Oral. The orally taken quick release preparation with micronized Iguratimod as active Form polar drugs have quite brittle, easily pulverized to fine crystals. 而难溶性. Immediate release oral diclofenac (50mg), thanks to its rapid and predictable absorption ensures fast relief of pain to GET over compliance issues. It is available.

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Enable Autosuggest. Previous Chapter. Next Chapter. AMA Citation Chapter Modified-Release Drug Products.

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Leon Shargel, et al. McGraw-Hill; Accessed June 01, MLA Citation. New York, NY: McGraw-Hill,http: Download citation file: RIS Zotero. Reference Manager.

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Several types of modified-release oral drug products are recognized: Sign In. Username Error: Please enter User Name. Password Error: