NDC 55513-150 - BLINCYTO

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: 55513-150
Package NDCs from labels: 55513-150-01
Manufacturer: Amgen, Inc
Effective date: 2026-04-14
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
BLINCYTO - Amgen, Inc	Amgen, Inc	2026-04-14	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55513-150-01	BLINCYTO	3.088 mL in 1 VIAL	INJECTION, POWDER, LYOPHILIZED,	3.088 mL	12.5 ug in 1mL	42

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55513-150	BLINCYTO (BLINATUMOMAB) KIT [AMGEN, INC]	40	Unmatched	20250511_38b482a8-960b-4591-9857-5031ecb830aa.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BLINATUMOMAB	ACTIVE INGREDIENT	4FR53SIF3A	BLINCYTO (BLINATUMOMAB) KIT [AMGEN INC]	7
BLINATUMOMAB	ACTIVE MOIETY	4FR53SIF3A	BLINCYTO (BLINATUMOMAB) KIT [AMGEN INC]	7
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	BLINCYTO (BLINATUMOMAB) KIT [AMGEN INC]	7
LYSINE HYDROCHLORIDE	INACTIVE INGREDIENT	JNJ23Q2COM	BLINCYTO (BLINATUMOMAB) KIT [AMGEN INC]	7
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	BLINCYTO (BLINATUMOMAB) KIT [AMGEN INC]	7
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	BLINCYTO (BLINATUMOMAB) KIT [AMGEN INC]	7
TREHALOSE DIHYDRATE	INACTIVE INGREDIENT	7YIN7J07X4	BLINCYTO (BLINATUMOMAB) KIT [AMGEN INC]	7

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 12 of 12 · 221 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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