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NDA 21-530/20-938 Oral Suspension: BPA SUMMARY CLINICAL PHARMACOLOGY AND BIOPHARMACEUTICS BPA SUMMARY REVIEW NDA 21-530/20-938 Brand Name: Generic Name: Dosage Form: Dosage Strength: Indication: NDA

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What is nda 21-53020-938 oral suspension?

NDA 21-53020-938 oral suspension is a medication in liquid form that is taken orally.

Who is required to file nda 21-53020-938 oral suspension?

The pharmaceutical company that manufactures nda 21-53020-938 oral suspension is required to file.

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NDA 21-53020-938 oral suspension should be filled out according to the instructions provided by the manufacturer or healthcare provider.

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The purpose of nda 21-53020-938 oral suspension is to administer medication in liquid form for easier ingestion and absorption.

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Information such as dosage instructions, potential side effects, and manufacturer details must be reported on nda 21-53020-938 oral suspension.

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