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CENTER FOR DRUG EVALUATION AND RESEARCH Approval Package for: APPLICATION NUMBER: 202570Orig1s000 Trade Name: Capsules, 200 mg and 250 mg. Generic Name: crizotinib Sponsor: Pfizer Inc. Approval Date:
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What is 202570orig1s000 - accessdata fda?
202570orig1s000 - accessdata fda is a unique identifier for a submission made to the FDA's accessdata platform.
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Companies or individuals submitting regulatory information to the FDA are required to file 202570orig1s000 - accessdata fda.
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To fill out 202570orig1s000 - accessdata fda, one must navigate to the FDA's accessdata platform, enter the required information, and submit the form according to the guidelines provided.
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The purpose of 202570orig1s000 - accessdata fda is to provide a standardized way for companies and individuals to submit regulatory information to the FDA for review.
What information must be reported on 202570orig1s000 - accessdata fda?
Information such as product details, testing results, and safety information must be reported on 202570orig1s000 - accessdata fda.
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