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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 212327
Company: BRISTOL-MYERS

Medication Guide

Products on NDA 212327

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
INREBIC	FEDRATINIB HYDROCHLORIDE	EQ 100MG BASE	CAPSULE;ORAL	Prescription	None	Yes	Yes

Approval Date(s) and History, Letters, Labels, Reviews for NDA 212327

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
08/16/2019	ORIG-1	Approval	Type 1 - New Molecular Entity	PRIORITY; Orphan	Label (PDF) Letter (PDF) Review		https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212327s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/212327Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2019/212327Orig1s000TOC.html

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
03/18/2026	SUPPL-9	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/212327s009lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2026/212327Orig1s009ltr.pdf
05/12/2025	SUPPL-7	Labeling-Package Insert, Labeling-Medication Guide	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/212327s007lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/212327Orig1s007ltr.pdf
07/30/2024	SUPPL-6	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/212327s006lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/212327Orig1s006ltr.pdf
05/15/2023	SUPPL-5	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/212327s005lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/212327Orig1s005ltr.pdf
11/23/2021	SUPPL-4	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/212327s004lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/212327Orig1s004ltr.pdf
12/03/2021	SUPPL-3	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/212327s003lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/212327Orig1s003ltr.pdf

Labels for NDA 212327

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
03/18/2026	SUPPL-9	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/212327s009lbl.pdf
05/12/2025	SUPPL-7	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/212327s007lbl.pdf
05/12/2025	SUPPL-7	Labeling-Medication Guide	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/212327s007lbl.pdf
07/30/2024	SUPPL-6	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/212327s006lbl.pdf
05/15/2023	SUPPL-5	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/212327s005lbl.pdf
12/03/2021	SUPPL-3	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/212327s003lbl.pdf
11/23/2021	SUPPL-4	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/212327s004lbl.pdf
08/16/2019	ORIG-1	Approval	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/212327s000lbl.pdf

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