NDC 71287-220-01 - TECARTUS

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 71287-220
Requested NDC: 71287-220-01
Package NDCs from labels: 71287-220-01, 71287-220-02
Manufacturer: Kite Pharma, Inc. | Gilead Sciences, Inc.
Effective date: 2026-06-16
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
TECARTUS - Kite Pharma, Inc. \| Gilead Sciences, Inc.	Kite Pharma, Inc. \| Gilead Sciences, Inc.	2026-06-16	CELLULAR THERAPY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71287-220-01	TECARTUS	68 mL in 1 BAG	SUSPENSION	68		16
71287-220-02	TECARTUS	1 in 1 PACKAGE	SUSPENSION	1		16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71287-220	TECARTUS (BREXUCABTAGENE AUTOLEUCEL) SUSPENSION [KITE PHARMA, INC.]	12	Current NDC, Legacy NDC, 2 package rows	20240627_a16108c2-7ca7-45af-965e-54bda4713022.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71287-220-01	EA - Each	71287-220	8fd9bcff-3c1b-4720-b28b-fcaadc68e0c5	1	2021-11-09
71287-220-02	EA - Each	71287-220	25e54ed8-ef75-420e-bad7-d7ad7e8d790b	1	2021-11-09

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 6 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dimethyl Sulfoxide	DIMETHYL SULFOXIDE	Renova Pharmaceuticals LLC	8f699de6-9d09-48da-9d95-4001d7008587	2026-07-20	Warnings, Adverse reactions	Exact identifier unii: YOW8V9698H
TECARTUS	BREXUCABTAGENE AUTOLEUCEL	Kite Pharma, Inc.	a16108c2-7ca7-45af-965e-54bda4713022	2026-06-16	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: BLA125703 ndc (package): 71287-220-01 ndc (package): 71287-219-01 ndc (package): 71287-219-02 ndc (package): 71287-220-02 ndc (product): 71287-220 ndc (product): 71287-219 ndc11 (package): 71287022001 rxcui: 2572002 rxcui: 2572005 rxcui: 2387347 rxcui: 2387352 spl id: 17c4a716-a22e-486d-b633-4be6c2453266 spl set id: a16108c2-7ca7-45af-965e-54bda4713022 unii: 4MD2J2T8SJ
Proteinuria Drops 2053	PROTEINURIA DROPS	Professional Complementary Health Formulas	1bf80282-8283-4835-acd4-fbdb47788c67	2026-01-08	Warnings	Exact identifier unii: ZIF514RVZR
ALBUMINEX	ALBUMIN HUMAN	BPL	8428d373-f4b1-4e3b-bb19-ea89048f7c79	2024-12-31	Warnings, Adverse reactions	Exact identifier unii: ZIF514RVZR
ALBUMINEX	ALBUMIN HUMAN	BPL	167f48d0-8ae5-4f7e-b050-9673dad78acc	2024-12-31	Warnings, Adverse reactions	Exact identifier unii: ZIF514RVZR
RIMSO-50	DIMETHYL SULFOXIDE	Mylan Institutional LLC	58b25d79-78f2-4953-b0c6-61658dc4ef0d	2021-03-17	Warnings, Adverse reactions	Exact identifier unii: YOW8V9698H

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.