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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 217700
Company: DAY ONE BIOPHARMS

Products on NDA 217700

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
OJEMDA	TOVORAFENIB	100MG	TABLET;ORAL	Prescription	None	Yes	Yes

Approval Date(s) and History, Letters, Labels, Reviews for NDA 217700

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
04/23/2024	ORIG-1	Approval	Type 1 - New Molecular Entity	PRIORITY; Orphan	Label (PDF) Letter (PDF) Review		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/217700s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/217700Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2024/217700Orig1s000, 218033Orig1s000TOC.html

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
08/27/2025	SUPPL-4	Labeling-Patient Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/217700s002s003s004lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/217700Orig1s002, s003, s004ltr.pdf
08/27/2025	SUPPL-3	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/217700s002s003s004lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/217700Orig1s002, s003, s004ltr.pdf
08/27/2025	SUPPL-2	Efficacy-New Patient Population	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/217700s002s003s004lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/217700Orig1s002, s003, s004ltr.pdf
06/26/2024	SUPPL-1	Labeling-Package Insert, Labeling-Patient Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/217700s001,218033s001lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/217700Orig1s001,218033Orig1s001ltr.pdf

Labels for NDA 217700

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
08/27/2025	SUPPL-4	Labeling-Patient Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/217700s002s003s004lbl.pdf
08/27/2025	SUPPL-3	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/217700s002s003s004lbl.pdf
08/27/2025	SUPPL-2	Efficacy-New Patient Population	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/217700s002s003s004lbl.pdf
06/26/2024	SUPPL-1	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/217700s001,218033s001lbl.pdf
06/26/2024	SUPPL-1	Labeling-Patient Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/217700s001,218033s001lbl.pdf
04/23/2024	ORIG-1	Approval	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/217700s000lbl.pdf

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