Regulations.gov document

Final Response Letter from FDA CDER to Reyoung Pharmaceutical Co., Ltd.

Other · FDA-2023-P-5675 · posted Feb 23, 2024

Key facts

Document ID FDA-2023-P-5675-0006
Title Final Response Letter from FDA CDER to Reyoung Pharmaceutical Co., Ltd.
Document type Other
Subtype Denial of Petition
Agency FDA
Docket FDA-2023-P-5675
Posted Feb 23, 2024
Comment period opens Feb 23, 2024

At a glance

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