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RECALL RESPONSE FORM TABLETS USP 300 mg, 500 Count Bottle NDC 0603211628VOLUNTARY RECALL RETAIL LEVEL PRODUCT DESCRIPTION Tablets USP 300 mg, 500 Counted NUMBER LOT # 0603211628 CP0761501EXP DATE
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01
Start by reading the instructions on the packaging or consult a healthcare professional for guidance.
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Wash your hands thoroughly before handling the tablets.
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Take one tablet and place it on a clean surface.
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Use a glass of water to help swallow the tablet. You may also consult the instructions to see if the tablet needs to be taken with food or on an empty stomach.
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Tilt your head back slightly and swallow the tablet with water. Avoid chewing or crushing the tablet unless instructed otherwise.
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If you have trouble swallowing the tablet, you may try breaking it in half or crushing it into smaller pieces as advised by your healthcare professional.
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Continue taking the prescribed dosage as instructed. Do not exceed the recommended dosage or frequency of intake without consulting a healthcare professional.
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Store the tablets in a cool, dry place as indicated on the packaging.

Who needs tablets usp 300 mg?

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Tablets USP 300 mg are typically prescribed for individuals who require a specific dosage of the active ingredient found in the tablets. It can only be determined by a healthcare professional based on the specific medical condition and needs of the patient. Therefore, it is important to consult a healthcare professional to determine if tablets USP 300 mg are suitable for you.
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Tablets USP 300 mg refers to a specific dosage form of medication that contains 300 milligrams of the active pharmaceutical ingredient.
Manufacturers or distributors of tablets USP 300 mg are required to file for approval and compliance with regulatory standards.
Filling out tablets USP 300 mg involves providing detailed information about the formulation, manufacturing process, quality control measures, and labeling of the medication.
The purpose of tablets USP 300 mg is to provide a specific and standardized dose of medication for therapeutic use.
Information that must be reported on tablets USP 300 mg includes the active ingredient, dosage strength, excipients, batch numbers, expiry dates, and manufacturing details.
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