CPC A61K 31/4164 (2013.01) [A61K 9/0053 (2013.01); A61K 47/02 (2013.01); A61K 47/14 (2013.01); A61K 47/26 (2013.01); A61K 47/38 (2013.01); A61K 47/46 (2013.01); A61P 31/04 (2018.01)] | 21 Claims |
1. An oral pharmaceutical liquid suspension comprising a) metronidazole or a pharmaceutically acceptable salt thereof; and b) magnesium aluminum silicate, wherein the magnesium aluminum silicate is a natural product.
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2. An oral pharmaceutical liquid suspension comprising a) metronidazole or a pharmaceutically acceptable salt thereof; b) magnesium aluminum silicate; and c) and at least one flavoring agent, wherein the magnesium aluminum silicate is a natural product.
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17. An oral pharmaceutical liquid suspension comprising: metronidazole, sucrose, glycerin, purified water, magnesium aluminum silicate, microcrystalline cellulose, sucralose, sodium phosphate, one or more preservatives, strawberry flavoring agent and peppermint flavoring agent, wherein the magnesium aluminum silicate is a natural product.
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18. A method of treating an infection in a patient, said method comprising the step of administering to the patient an effective amount of an oral pharmaceutical liquid suspension comprising:
a) metronidazole or a pharmaceutically acceptable salt thereof and magnesium aluminum silicate; or
b) metronidazole or a pharmaceutically acceptable salt thereof; magnesium aluminum silicate; and at least one flavoring agent;
wherein the magnesium aluminum silicate is a natural product.
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