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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 214094
Company: BIOCRYST

Products on NDA 214094

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
ORLADEYO	BEROTRALSTAT DIHYDROCHLORIDE	EQ 110MG BASE	CAPSULE;ORAL	Prescription	None	Yes	No
ORLADEYO	BEROTRALSTAT DIHYDROCHLORIDE	EQ 150MG BASE	CAPSULE;ORAL	Prescription	None	Yes	Yes

Approval Date(s) and History, Letters, Labels, Reviews for NDA 214094

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
12/03/2020	ORIG-1	Approval	Type 1 - New Molecular Entity	STANDARD; Orphan	Label (PDF) Letter (PDF) Review		https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/214094s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/214094Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2020/214094Orig1s000TOC.cfm

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
12/23/2025	SUPPL-5	Labeling-Package Insert, Labeling-Patient Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/214094s005lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/214094Orig1s005ltr.pdf
10/21/2024	SUPPL-3	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/214094s003lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/214094Orig1s003ltr.pdf
11/21/2023	SUPPL-2	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/214094s002lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/214094Orig1s002ltr.pdf

Labels for NDA 214094

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
12/23/2025	SUPPL-5	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/214094s005lbl.pdf
12/23/2025	SUPPL-5	Labeling-Patient Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/214094s005lbl.pdf
10/21/2024	SUPPL-3	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/214094s003lbl.pdf
11/21/2023	SUPPL-2	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/214094s002lbl.pdf
12/03/2020	ORIG-1	Approval	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/214094s000lbl.pdf

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