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 65 of 89 · 1,774 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Isopropyl Rubbing Alcohol 70%	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	a9960d2f-f13a-4168-b2e9-d6f4a35d84ae	2024-10-21	Warnings	Exact identifier unii: ND2M416302
Isopropyl Rubbing Alcohol 50%	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	5db1659e-3a13-47f0-90ae-f8f192c6111a	2024-10-21	Warnings	Exact identifier unii: ND2M416302
Isopropyl Rubbing Alcohol 70% with Wintergreen	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	3dcdc1cc-ece8-4b47-a236-ee57c375bb99	2024-10-21	Warnings	Exact identifier unii: ND2M416302
Isopropyl Rubbing Alcohol 50% with Wintergreen	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	0b185535-b1af-4128-89ca-65b0e63cd430	2024-10-21	Warnings	Exact identifier unii: ND2M416302
Rhustoxoforce	APIS MELLIFICA, CANTHARIS, GRAPHITES, NATRUM MURIATICUM, RHUS GLABRA, RHUS TOXICODENDRON, RHUS VENENATA, URTICA DIOICA	BioActive Nutritional, Inc.	5a3627f1-a850-42f3-8c7a-b2067bd03538	2024-10-18	Warnings	Exact identifier unii: 451W47IQ8X
LACTATED RINGERS	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Becton Dickinson and Company	bb2ad9cd-5d9a-4337-be61-0842d738c79e	2024-10-16	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Elliotts B	SODIUM CATION, SODIUM BICARBONATE, ANHYDROUS DEXTROSE, MAGNESIUM SULFATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM PHOSPHATE	Lukare Medical, LLC	08036dbd-55b3-47b9-9890-000f253544f3	2024-10-16	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
LACTATED RINGERS	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Fresenius Kabi USA, LLC	8fce1477-991f-4b43-bf05-a80bad897262	2024-10-16	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
IDACIO	ADALIMUMAB-AACF	Fresenius Kabi USA, LLC	08dbaffe-9d05-43cf-b24b-b44ade8685fc	2024-10-15	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 797544
Genuine First Aid Alcohol Cleansing Pad	ISOPROPYL ALCOHOL	GFA Production (Xiamen) Co., Ltd.	af090168-f9b3-c2fa-e053-2a95a90a1b76	2024-10-15	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
EyS Eye Wash	WATER	Eyes-Plus LLC	1443f6bf-3a77-4a19-8585-0ec58efe042f	2024-10-15	Warnings	Exact identifier unii: 059QF0KO0R
Eye Wash	WATER SOLUTION	Kroger Company	354402ad-581d-47e7-9fd3-933bef281ff4	2024-10-11	Warnings	Exact identifier unii: 059QF0KO0R
Isopropyl Alcohol Cleansing Pad	ISOPROPYL ALCOHOL	Hubei Changjian Medical Products Co., Ltd.	e6f9a23b-ae6e-4fce-b66d-b602038dc746	2024-10-11	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
Eye Wash	WATER	Hubei Changjian Medical Products Co., Ltd.	d57e1c5b-1edc-4a94-88bc-f9ecf347b7ea	2024-10-11	Warnings	Exact identifier unii: 059QF0KO0R
Sodium Chloride	SODIUM CHLORIDE	Fresenius Kabi USA, LLC	c44b0fdb-33df-4747-b443-5fb4deb456cb	2024-10-11	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Bacteriostatic Sodium Chloride	SODIUM CHLORIDE	Fresenius Kabi USA, LLC	e5e325d1-0d58-40c9-9645-3ae402ff9d92	2024-10-11	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Vamousse Lice Defense	EUCALYPTUS GLOBULUS, NATRUM MURIATICUM	Alliance Pharma Inc.	c87ce5d3-c200-421e-88be-bc8060a5993a	2024-10-08	Warnings	Exact identifier unii: 451W47IQ8X
Physicians EZ Use B-12 Compliance	PHYSICIANS EZ USE B-12 COMPLIANCE	Asclemed USA, Inc.	168f94ea-2faf-4aeb-88a5-8753ad60a1c4	2024-10-05	Warnings, Adverse reactions	Exact identifier rxcui: 797544
Enoxiluv Kit	ENOXAPARIN SODIUM, ISOPROPYL ALCOHOL	Asclemed USA, Inc.	e8855fae-f70d-4099-969e-a1d9f2929259	2024-10-05	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 797544
Dyural 80-LM	METHYLPREDNISOLONE ACETATE, LIDOCAINE HYDROCHLORIDE, BUPIVACAINE HYDROCHLORIDE, POVIDINE IODINE, ISOPROPYL ALCOHOL	Asclemed USA, Inc.	c4071146-7d89-4c3a-9278-389d801cf66d	2024-10-05	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 797544

Reported adverse events (FAERS/openFDA)#

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