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 63 of 89 · 1,774 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
70% ISOPROPYL RUBBING ALCOHOL	ISOPROPYL ALCOHOL	MY IMPORTS USA LLC	26cbc1af-a38f-146b-e063-6394a90a716c	2024-11-13	Warnings	Exact identifier unii: ND2M416302
Sodium Chloride	SODIUM CHLORIDE	Baxter Healthcare Company	99a15716-bbb9-4e33-a48d-20c58b81f392	2024-11-13		Exact identifier unii: 451W47IQ8X
Adalimumab-adbm	ADALIMUMAB-ADBM	QUALLENT PHARMACEUTICALS HEALTH LLC	f9986706-9c75-4335-a54f-09d7716dbcef	2024-11-12	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 797544
Itch Formula	ANTIPYRINUM, APIS MELLIFICA, CALENDULA OFFICINALIS, CANTHARIS, COPAIVA OFFICINALIS, CROTON TIGLIUM, GRAPHITES, HISTAMINUM HYDROCHLORICUM, LEDUM PALUSTRE, MEZEREUM, NATRUM MURIATICUM, PETROLEUM, RHUS VENENATA, STAPHYSAGRIA, SULPHUR, URTICA URENS	Deseret Biologicals, Inc.	4dfb177b-bff3-4b6d-8fd9-cadd1df7812c	2024-11-12	Warnings	Exact identifier unii: 451W47IQ8X
Plasma-Lyte 148 (pH 7.4)	SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE	Baxter Healthcare Corporation	fe935c8d-f42d-42e4-8665-0dc66829f231	2024-11-08		Exact identifier unii: 02F3473H9O unii: 451W47IQ8X
Crane Safety Eye Wash	WATER SOLUTION	Crane Safety LLC	96d8dda9-6cd6-3f68-e053-2995a90a0da2	2024-11-08	Warnings	Exact identifier unii: 059QF0KO0R
Klean Detox	AESCULUS HIPPOCASTANUM, EQUISETUM HYEMALE, HYDRASTIS CANADENSIS, HYDROCOTYLE ASIATICA, LINUM USITATISSIMUM, MAGNESIA MURIATICA, PASSIFLORA INCARNATA, SOLIDAGO VIRGAUREA, THUJA OCCIDENTALIS, FUMARIA OFFICINALIS, ONONIS SPINOSA	Ratis, LLC	aea99daf-7de4-4c85-b2b6-735ef095af2e	2024-11-08	Warnings	Exact identifier unii: 02F3473H9O
RUGBY EYE WASH	WATER, PURIFIED	A-S Medication Solutions	0773e558-2f46-494c-888a-3bc517202b65	2024-11-08	Warnings	Exact identifier unii: 059QF0KO0R
Barbie ALCOHOL WIPE	ISOPROPYL ALCOHOL	Ashtel Studios, Inc.	a4a6beb0-5781-4d74-9120-7ca64e035c23	2024-11-08	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
MARVEL ALCOHOL WIPE	ISOPROPYL ALCOHOL	Ashtel Studios, Inc.	f6cd4757-d6e0-46bd-827f-3f380c71858f	2024-11-07	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE	BECTON DICKINSON AND COMPANY	d3f90d2f-4536-4d32-800b-7a798f8a35db	2024-11-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	Hospira, Inc.	8eb172da-dcd4-4660-4a8f-ad44a14b4af7	2024-11-06	Adverse reactions	Exact identifier unii: 451W47IQ8X
Licefreee Everyday	SODIUM CHLORIDE	Tec Laboratories,Inc.	407b5fd6-2331-2ba7-e054-00144ff88e88	2024-11-05	Warnings	Exact identifier unii: 451W47IQ8X
Licefreee	HEAD LICE TREATMENT	Tec Laboratories, Inc.	08c9d3dd-7177-0148-e054-00144ff8d46c	2024-11-05	Warnings	Exact identifier unii: 451W47IQ8X
Bladder Relief	CAUSTICUM, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (VULGARIS), SEPIA, STAPHYSAGRIA, THUJA OCCIDENTALIS	Magni Company	5d0db70c-6360-493b-bcf2-8dbc95314140	2024-11-05	Warnings	Exact identifier unii: 451W47IQ8X
Vaccines	ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, MORBILLINUM, NATRUM MURIATICUM, SILICEA, SULPHUR IODATUM, THUJA OCCIDENTALIS, URTICA URENS	Liddell Laboratories, Inc.	6e6e67d4-089e-4775-b4a4-5511953f6e3f	2024-11-04	Warnings	Exact identifier unii: 451W47IQ8X
Gluten Detox	BARLEY (GRAIN), CARBO VEGETABILIS, CINCHONA OFFICINALIS, GLUTEN, GLYPHOSATE, HYDRASTIS CANADENSIS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA, OAT (GRAIN), PANCREAS SUIS, PULSATILLA (VULGARIS), RYE (GRAIN), WHEAT (GRAIN)	Liddell Laboratories, Inc.	706f2e33-8674-4911-ba0a-4efc935e7739	2024-11-04	Warnings	Exact identifier unii: 451W47IQ8X
Derma Pain	CALENDULA OFFICINALIS, CROTON TIGLIUM, NATRUM MURIATICUM, PLANTAGO MAJOR, RHUS TOX, SARSAPARILLA (SMILAX REGELII)	Liddell Laboratories, Inc.	e02a5e99-aa27-4276-a785-7b5328d89fdc	2024-11-04	Warnings	Exact identifier unii: 451W47IQ8X
Alcohol Prep Pad	ALCOHOL PREP PAD	ASO LLC	7481bfb9-2baf-b1ec-e053-2991aa0ad2de	2024-11-01	Warnings	Exact identifier unii: ND2M416302
Alcohol Prep Pad	ALCOHOL PREP PAD	ASO LLC	f2a41151-a807-566c-e053-2995a90af877	2024-11-01	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

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