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 12 of 90 · 1,798 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DOUE 50% ISOPROPYL RUBBING ALCOHOL	ISOPROPYL ALCOHOL	ONEST LIMITED	414baa60-6af1-4966-9580-ce7871ab7142	2026-05-01	Warnings	Exact identifier unii: ND2M416302
DOUE 50% ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN	ISOPROPYL ALCOHOL	ONEST LIMITED	fe008352-0643-4aa7-ae04-883c58832285	2026-05-01	Warnings	Exact identifier unii: ND2M416302
Redicare Alcohol Prep Pads	MEDIUM ALCOHOL PREP PADS	Redicare LLC	3cb7fba1-1d2d-f4da-e063-6394a90a4b21	2026-05-01	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
70%	ISOPROPYL ALCOHOL	Your Military Exchanges	3dcb8422-827d-479b-ba18-eee8dbb762e1	2026-04-30	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Perrigo Direct, Inc	11d89d11-103e-4ef6-a996-65cff67f9b32	2026-04-29	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Walmart Inc.	1fd3d29f-7da0-c5ba-e063-6294a90add16	2026-04-29	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Sodium Chloride	SODIUM CHLORIDE	Sportpharm LLC	a2c111f6-74d5-4a5d-82ac-d0f237488cb8	2026-04-24	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
leuprolide acetate	LEUPROLIDE ACETATE	Sun Pharmaceutical Industries, Inc.	a3b01473-30c7-4945-bd60-2484221aaaad	2026-04-24	Warnings, Adverse reactions	Exact identifier rxcui: 797544
Leuprolide Acetate	LEUPROLIDE ACETATE	Meitheal Pharmaceuticals Inc	d6bd26bd-b8d8-4c5a-bc5c-7b8a1efaa584	2026-04-23	Warnings, Adverse reactions	Exact identifier rxcui: 797544
Sodium Chloride	SODIUM CHLORIDE	Method Pharmaceuticals, LLC	4b08859e-65bd-8255-e063-6394a90af614	2026-04-23	Warnings	Exact identifier unii: 451W47IQ8X
3M DuraPrep Surgical	IODINE POVACRYLEX AND ISOPROPYL ALCOHOL	Solventum US LLC	22a10a54-6a04-48b3-9ec4-b26526183daf	2026-04-23	Warnings	Exact identifier unii: ND2M416302
3M SoluPrep S	CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL	Solventum US LLC	084aa305-5863-441a-a94d-36bc1b05195a	2026-04-23	Warnings	Exact identifier unii: ND2M416302
Ringers	SODIUM CHLORIDE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE	ICU Medical, Inc.	a926f913-18fa-4a3e-bfd6-210e1e427960	2026-04-20	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Cardioforce II	ABROTANUM, BOLDO, CIMICIFUGA RACEMOSA, KALI PHOSPHORICUM, TARAXACUM OFFICINALE, CONVALLARIA MAJALIS, MAGNESIA SULPHURICA, OLEANDER, NATRUM MURIATICUM, BELLIS PERENNIS	BioActive Nutritional, Inc.	733bbb26-7698-4a1b-9dc8-7e3490ffc92b	2026-04-17	Warnings	Exact identifier unii: 451W47IQ8X
Thyroid HP	BARYTA CARBONICA, CALCAREA CARBONICA, FUCUS VESICULOSUS, IODIUM, NATRUM MURIATICUM, PULSATILLA, SPONGIA TOSTA, THYROIDINUM (SUIS)	BioActive Nutritional, Inc.	3795820a-cf2a-4094-9a02-70e3757b7510	2026-04-17	Warnings	Exact identifier unii: 451W47IQ8X
DIANEAL Low Calcium with Dextrose	SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE	Vantive US Healthcare LLC	aa268d3f-7389-4f25-801f-5d4825495f08	2026-04-16	Warnings, Adverse reactions	Exact identifier unii: 02F3473H9O unii: 451W47IQ8X
PEG 3350 and Electrolytes	POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE	Wilshire Pharmaceuticals, Inc.	b251752d-7750-482a-9364-0acf4ad47cc8	2026-04-16	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE	Fresenius Kabi USA, LLC	99c6a1a9-cadf-435b-a332-ccc189afdfa9	2026-04-16	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
ALCOHOL PREP PADS LARGE STERILE	ISOPROPYL ALCOHOL CLOTH	JINHUA JINGDI MEDICAL SUPPLIES CO.,LTD	4f8ba6c8-5155-c491-e063-6394a90adde9	2026-04-15	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
GoLYTELY	POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE	Azurity Pharmaceuticals, Inc.	7609ecf7-0ce0-4fbb-9c27-30987f689575	2026-04-15	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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