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Drugs@FDA: FDA-Approved Drugs

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Biologic License Application (BLA): 761202
Company: SAMSUNG BIOEPIS CO LTD

Products on BLA 761202

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
BYOOVIZ	RANIBIZUMAB-NUNA	0.5MG(10MG/ML)	INJECTABLE;INJECTION	Prescription	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for BLA 761202

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
09/17/2021	ORIG-1	Approval		N/A	Label (PDF) Letter (PDF) Review		https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/761202s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/761202Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2021/761202Orig1s000TOC.html

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
03/30/2026	SUPPL-19	Supplement	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/761202s019lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2026/761202Orig1s019ltr.pdf
11/12/2025	SUPPL-17	Supplement	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/761202s017lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/761202Orig1s017ltr.pdf
08/15/2025	SUPPL-16	Supplement	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/761202s016lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/761202Orig1s016ltr.pdf
06/16/2023	SUPPL-7	Supplement	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/761202Orig1s007Lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/761202Orig1s007ltr.pdf
10/03/2023	SUPPL-6	Supplement	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/761202s006lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/761202Orig1s006ltr.pdf
06/09/2022	SUPPL-4	Supplement	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/761202s004lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2022/761202Orig1s004ltr.pdf
08/15/2022	SUPPL-3	Supplement	Letter (PDF)	Label is not available on this site.	https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2022/761202Orig1s003ltr.pdf

Labels for BLA 761202

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
03/30/2026	SUPPL-19	Labeling-Container/Carton Labels	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/761202s019lbl.pdf
03/30/2026	SUPPL-19	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/761202s019lbl.pdf
11/12/2025	SUPPL-17	Labeling-Container/Carton Labels	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/761202s017lbl.pdf
11/12/2025	SUPPL-17	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/761202s017lbl.pdf
08/15/2025	SUPPL-16	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/761202s016lbl.pdf
10/03/2023	SUPPL-6	Efficacy-Labeling Change With Clinical Data	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/761202s006lbl.pdf
06/16/2023	SUPPL-7	Labeling-Patient Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/761202Orig1s007Lbl.pdf
06/09/2022	SUPPL-4	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/761202s004lbl.pdf
09/17/2021	ORIG-1	Approval	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/761202s000lbl.pdf

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