NDC 71894-110 - Zolgensma

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: 71894-110
Package NDCs from labels: 71894-110-01
Manufacturer: Novartis Innovative Technologies 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
Zolgensma - Novartis Innovative Technologies Inc.	Novartis Innovative Technologies Inc.	2026-06-16	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71894-110	ZOLGENSMA (ONASEMNOGENE ABEPARVOVEC-XIOI) KIT [NOVARTIS GENE THERAPIES, INC.]	13	Unmatched	20250214_68cd4f06-70e1-40d8-bedb-609ec0afa471.zip

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 6 of 90 · 1,798 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sodium Chloride	SODIUM CHLORIDE	LABORATORIOS GRIFOLS SA	eb811d79-fdb8-1f1a-c2ad-1cc4bfc7eadf	2026-07-15	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Yuflyma	ADALIMUMAB-AATY	CELLTRION USA, Inc.	526d626f-8c9f-496c-b838-00a73bb36383	2026-07-15	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 797544
WHWSWB 0.9% SALINE	SODIUM CHLORIDE	Yiwu Huanshu E-commerce Co., Ltd	5082b773-79b2-2501-e063-6394a90a170f	2026-07-11	Warnings	Exact identifier unii: 451W47IQ8X
Alcohol Cleansing Wipe	ISOPROPYL ALCOHOL	Hubei Fanjian Medical Product Co.,Ltd	1607fb06-826b-42bb-986e-0023a1b078f3	2026-07-10	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
Walgreens	DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, LIDOCAINE HCL, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, ETHYL ALCOHOL	Walgreen Co.	5630f48b-404c-b847-e063-6394a90a8d8e	2026-07-09	Warnings	Exact identifier rxcui: 797544
Nervionix Pro Magnesium Ice	LIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDE	Micelle Laboratories, Incorporated	c11e0963-90fb-48c6-938a-3dcbbad17aca	2026-07-09	Warnings	Exact identifier unii: 02F3473H9O
Adalimumab	ADALIMUMAB-AATY	CELLTRION USA, Inc.	c44365e9-d470-4e35-978d-8565a9e3471e	2026-07-08	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 797544
Freskaro Ear Drops for Swimmers	FRESKARO EAR DROPS FOR SWIMMERS	Pharma Nobis, LLC	4f724d85-cd38-41da-e063-6394a90a9fd7	2026-07-08	Warnings	Exact identifier unii: ND2M416302
Care Science	DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, LIDOCAINE HCL, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, ETHYL ALCOHOL	ASO LLC	562f2b2c-d234-e491-e063-6294a90a705f	2026-07-08	Warnings	Exact identifier rxcui: 797544
SALINE NASAL	SODIUM CHLORIDE	ALAINA HEALTHCARE PRIVATE LIMITED	ed30a7f9-7132-42da-9bed-63a9b1c80ab2	2026-07-07	Warnings	Exact identifier unii: 451W47IQ8X
70%	ISOPROPYL ALCOHOL	Save-A-Lot Food Stores Ltd	a592326c-c062-4ebf-b8dd-83f7e6f2f22b	2026-07-07	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g)	NMN (NICOTINAMIDE MONONUCLEOTIDE), ECTOIN (ECTOINE)	Reedfresh Co., LTD	55d703ca-ff9d-0dbc-e063-6294a90ab6b1	2026-07-05	Warnings	Exact identifier unii: 059QF0KO0R
Eyesaline Eyewash Concentrate	PURIFIED WATER	Protective Industrial Products, Inc.	558e5926-9027-d3f6-e063-6294a90ab121	2026-07-02	Warnings	Exact identifier unii: 059QF0KO0R
Fendall 2000 Pure Flow	PURIFIED WATER	Protective Industrial Products, Inc.	55a1d07e-0006-0c75-e063-6394a90a7acc	2026-07-02	Warnings	Exact identifier unii: 059QF0KO0R
Fendall 1000 Pure Flow	PURIFIED WATER	Protective Industrial Products, Inc.	55a2f4da-bb1e-8ead-e063-6394a90af72e	2026-07-02	Warnings	Exact identifier unii: 059QF0KO0R
Sterile Eyesaline Eyewash	STERILE EYESALINE EYEWASH	Protective Industrial Products, Inc.	55a290e8-8310-8be4-e063-6394a90abdce	2026-07-02	Warnings	Exact identifier unii: 059QF0KO0R
Eyesaline Emergency Eyewash	PURIFIED WATER	Protective Industrial Products, Inc.	55a261c2-725d-6765-e063-6294a90a3260	2026-07-02	Warnings	Exact identifier unii: 059QF0KO0R
Remodulin	TREPROSTINIL	United Therapeutics Corporation	6c80bb38-e8db-4138-9f0d-dbbf9c673185	2026-07-02	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
The Cell Salt Co. Daily Blend 12 in 1	CALC FLUOR, CALC PHOS, CALC SULPH, FERRUM PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT MUR, NAT PHOS, NAT SULPH, SILICEA	The Cell Salt Company LLC	55826f59-acf4-7370-e063-6394a90afed7	2026-07-01	Warnings	Exact identifier unii: 451W47IQ8X
OHTrust Artifical Eyedrop	SODIUM CHLORIDE	Nanoplus Technology Co., Limited	2ea26d96-704b-17bb-e063-6394a90a7e27	2026-07-01	Warnings	Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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