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3. An amniotic membrane powder composition comprising an amount of elastin in the range of 4 mg/g to 100 mg/g. 4. The composition of claim 2, wherein the elastin is in in the range of 5 mg/g to 60 mg/g. 5. An amniotic membrane powder composition comprising an amount of collagen in the range of 10 mg/g to 800 mg/g. 6.
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Nov 01, 2021·The empirical formula is C 14 H 21 N 3 O 2 S, representing a molecular weight of 295.4. Sumatriptan is a white to off-white powder that is very slightly soluble in water and in saline. Each Sumatriptan Nasal Spray contains 20 mg of sumatriptan in a 100-MicroL unit dose aqueous buffered solution containing monobasic potassium phosphate NF, anhydrous dibasic …
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Jan 01, 2021·Liquid dosage forms have been widely applied in the pharmaceutical industry, with their applications ranging from oral preparations and injectables all the way through otic, nasal, rectal, and vaginal formulations. This chapter outlines the different types of liquid dosage forms, comparing their individual constituents and discussing their main ...
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In the United States (U.S.) sumatriptan is approved by the Food and Drug Administration (FDA) as a human prescription drug. In the U.S., sumatriptan products are available in tablet, injection, subcutaneous injection and nasal spray/powder dosage forms. Sumatriptan (as sumatriptan succinate) was the first triptan approved by the FDA in 1992.
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Thus, sumatriptan 25 mg, 50 mg, and 100 mg were prepared that were taste-masked with an Amberlite™ IRP88N resin. Example 3 Following the method set out in Example 1, drug-resin complexes of guaifenesin granules were prepared by making appropriate changes to the formulation of Example 1.
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