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 68 of 89 · 1,774 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Derma Pain Plus	CROTON TIGLIUM, NATRUM MURIATICUM, PLANTAGO MAJOR, RHUS TOXICODENDRON, SARSAPARILLA (SMILAX REGELII)	Peaceful Mountain, Inc.	6fa79c31-e48e-4c83-baa2-96cef22cfee1	2024-06-13	Warnings	Exact identifier unii: 451W47IQ8X
Cold Sore Rescue	BORAX, DULCAMARA, NATRUM MURIATICUM, RANUNCULUS BULBOSUS, SILICEA	Peaceful Mountain, Inc.	a7fe6ec7-a758-43cf-b46f-c327e0632fb8	2024-06-13	Warnings	Exact identifier unii: 451W47IQ8X
Swabs	ISOPROPYL ALCOHOL	McKesson	4650c945-8e38-5ad9-e054-00144ff8d46c	2024-06-07	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
Eyes Alive Eye Wash	WATER	RIVIERA PHARMA INC	081079f4-1c06-4054-b771-00fedaa666f6	2024-06-05	Warnings	Exact identifier unii: 059QF0KO0R
NATRUM MUR	NATRUM MUR	Rxhomeo Private Limited d.b.a. Rxhomeo, Inc	1a22655a-68f3-4f13-e063-6294a90ae52c	2024-06-05	Warnings	Exact identifier unii: 451W47IQ8X
Sterile Water	WATER	Becton Dickinson and Company	6e43c5a3-dad2-49ed-b500-964cb4563cc9	2024-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Mentox HP	AURUM METALLICUM, BARYTA CARBONICA, CALCAREA CARBONICA, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA, PHOSPHORUS	Energique, Inc.	ebb23637-4931-4563-ab30-99bea0276580	2024-05-28	Warnings	Exact identifier unii: 451W47IQ8X
Potassium Chloride in Lactated Ringers and Dextrose	POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM LACTATE, AND DEXTROSE MONOHYDRATE	Fresenius Kabi USA, LLC	dbed53b7-0109-4561-8342-0178ec8c64b0	2024-05-22	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Lactated Ringers and Dextrose	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE	Fresenius Kabi USA, LLC	1b912c7e-f005-4af4-b683-083440964249	2024-05-22	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sodium chloride	SODIUM CHLORIDE	Fresenius Kabi USA, LLC	239a5af1-7498-480f-862c-ab7c3d89d183	2024-05-21	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sodium chloride	SODIUM CHLORIDE	Becton Dickinson and Company	ebc8b008-a8b3-4c41-89e4-b413f7aab89f	2024-05-21	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Allergies	APIS MELLIFICA, ECHINACEA, HYDRASTIS CANADENSIS, TARAXACUM OFFICINALE, ACONITUM NAPELLUS, AETHUSA CYNAPIUM, AGARICUS MUSCARIUS, ALETRIS FARINOSA, ALFALFA, ALLIUM CEPA, ALLIUM SATIVUM, AMBROSIA ARTEMISIAEFOLIA, ARSENICUM ALBUM, ARTEMISIA VULGARIS, ARUNDO MAURITANICA, AVENA SATIVA, BELLADONNA, BELLIS PERRENIS, BOVISTA, BROMIUM, BRYONIA, CAFFEINUM, CALCAREA CARBONICA, CALLUNA VULGARIS, FLOS, CAPSICUM ANNUUM, CAT HAIR, CHAMOMILLA, CHELIDONIUM MAJUS, CHENOPODIUM ANTHELMINTICUM, CINNAMOMUM	Newton Laboratories, Inc.	9d5dea47-5103-21a3-e053-2995a90aee78	2024-05-20	Warnings	Exact identifier unii: 451W47IQ8X
Colopar	COLON (SUIS), ARSENICUM ALBUM, CAUSTICUM, IGNATIA AMARA, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA, SEPIA, SILICEA, THUJA OCCIDENTALIS	Energique, Inc.	c47d7203-abcd-4ae5-bf9b-5df07e07d3c1	2024-05-20	Warnings	Exact identifier unii: 451W47IQ8X
HUMIRA	ADALIMUMAB	A-S Medication Solutions	a06a9aec-fd5b-4c3e-a81f-eb46bb384100	2024-05-16	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 797544
Aging Eye Formula	CINERARIA MARITIMA, EYE (SUIS), CALCAREA FLUORICA, CAUSTICUM, GERMANIUM METALLICUM, PHOSPHORUS, SILICEA, ZINCUM METALLICUM, NATRUM MURIATICUM	Nutritional Specialties, Inc.	4510fe59-cc28-4585-925f-42508a60abd0	2024-05-13	Warnings	Exact identifier unii: 451W47IQ8X
Debrox Kids	ISOPROPYL ALCOHOL	Medtech Products Inc.	f42eee70-c4ee-44ad-85d5-a06d98ecb8b0	2024-05-09	Warnings	Exact identifier unii: ND2M416302
Sodium Chloride	SODIUM CHLORIDE	B. Braun Medical Inc.	47a0313f-36df-4fa6-a828-c9e1946ba9b0	2024-05-08	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Potassium Chloride in Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, AND POTASSIUM CHLORIDE	Fresenius Kabi USA, LLC	f0cc6713-4d47-49be-8116-901c99002b6b	2024-05-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	B. Braun Medical Inc.	7f22c06b-6b4d-4b49-a4b2-d2169f2bd653	2024-05-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE	Asclemed USA, Inc.	f4ca52c6-9f90-7bb5-e053-2a95a90ae3ff	2024-05-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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