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Where the FDA does approve a drug, it reviews the drug's safety data and allows later trials or more supervision. The FDA has also created the "approval review" process that allows for an additional trial delay. Level I issues, such as an extended exclusivity or a generic drug's prior approval, are sufficient to establish a drug's safety profile. When reviewing a drug, the FDA considers information such as its manufacturing process, drug composition, and drug strength and dosage form. It also considers its associated shelf-life and drug-availability information to ensure that the drug is safe and effective in treating a serious disease or condition. Available as a generic or a prescription, generic drugs are available at a lower cost than prescription medications. An FDA-approved drug product is manufactured according to FDA-approved manufacturing standards. Generic drugs typically cost less than the prescription prescription reference drug price, because the FDA itself doesn't pay for the newly manufactured drug until the drug passes background checks. Also, the price of the drug is low because it's more expensive to run the FDA's Food, Drug, and Cosmetic Supplements (FDA) than it is to run a drug's FDA and drug-drug interactions. FDA-approved drugs can be manufactured in the United States, and FDA monitors the quality of these products to ensure they meet the highest potential for abuse and liability. No, it's not because the drugs are FDA-approved. It's because the drugs are FDA-approved drugs that are approved by the FDA, and are thus being manufactured in the United States. There are also some subtle differences and disadvantages between the drugs, but these differences are better explained by the differences in FDA certification and other factors. clotrimazole 100mg prescription assistance program
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