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
LabelManufacturerEffective dateType
Zolgensma - Novartis Innovative Technologies Inc.Novartis Innovative Technologies Inc.2026-06-16HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION11.0 mL20000000000000 [arb'U] in 1mL14
71894-110-01Zolgensma5.5 mL in 1 VIALINJECTION, SUSPENSION5.5 mL20000000000000 [arb'U] in 1mL14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71894-110ZOLGENSMA (ONASEMNOGENE ABEPARVOVEC-XIOI) KIT [NOVARTIS GENE THERAPIES, INC.]13Unmatched20250214_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 39 of 89 · 1,774 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
American Red Cross 70% Isopropyl AlcoholISOPROPYL ALCOHOL(70%CONC.)Zhejiang Guoyao Jingyue Aerosol Co., Ltd.41b6ee3f-55f4-0502-e063-6394a90aa3572025-10-21WarningsExact identifier
unii: ND2M416302
CVS Alcohol PrepISOPROPYL ALCOHOLCVS Pharmacy7abc66f2-faf6-421c-9c3c-b69f5a5872462025-10-20WarningsExact identifier
rxcui: 797544
unii: ND2M416302
PROHEAL ALCOHOL XXL PREP PADSISOPROPYL ALCOHOLClick Industries LLCec81be59-94a5-4675-9047-e3e82d7ad7612025-10-20WarningsExact identifier
rxcui: 797544
unii: ND2M416302
ALCOHOL PREP PADISOPROPYL ALCOHOLGuangdong Comfort Medical Products Co., Ltd.3a2dea43-8123-3fb7-e063-6294a90a5e502025-10-19WarningsExact identifier
rxcui: 797544
unii: ND2M416302
ChloraPrep One-StepCHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOLCareFusion 213, LLC85790749-5a95-7f18-e053-2a91aa0a1a022025-10-17WarningsExact identifier
unii: ND2M416302
ChloraPrep One-StepCHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOLCareFusion 213, LLC85791e13-4103-19fe-e053-2991aa0a647f2025-10-17WarningsExact identifier
unii: ND2M416302
ChloraPrep One-StepCHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOLCareFusion 213, LLC85794f6b-d1ea-40f9-e053-2991aa0a88232025-10-17WarningsExact identifier
unii: ND2M416302
WalgreensSODIUM CHLORIDEWalgreen Company21dfc2cf-65ae-c3fb-e063-6294a90a0a942025-10-17Exact identifier
unii: 451W47IQ8X
ChloraPrep SwabstickCHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOLCareFusion 213 LLC1666069b-38f6-bfde-e063-6394a90ad1b82025-10-17WarningsExact identifier
unii: ND2M416302
Medline Alcohol Prep Sterile, LargeISOPROPYL ALCOHOLMedline Industries, LPc9fae7b6-2f4b-490b-9b17-a7297e7380692025-10-16WarningsExact identifier
rxcui: 797544
unii: ND2M416302
Medline Alcohol Prep Sterile, MediumISOPROPYL ALCOHOLMedline Industries, LP9a8584e1-b422-4b77-8464-4e022d578fad2025-10-16WarningsExact identifier
rxcui: 797544
unii: ND2M416302
Medline Alcohol PrepISOPROPYL ALCOHOLMedline Industries, LPb43c0bff-82f8-c18d-e053-2995a90a87162025-10-16WarningsExact identifier
rxcui: 797544
unii: ND2M416302
SimlandiADALIMUMAB-RYVKA-S Medication Solutionsba9dd71c-13c9-4cfe-84a2-b4f17d1c583f2025-10-16Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 797544
Homeopathic Tea Tree Oil LiceEUCALYPTUS GLOBULUS, NATRUM MURIATICUMDOLGENCORP, LLC0a0c2db2-7eeb-909c-e063-6394a90a7a902025-10-15WarningsExact identifier
unii: 451W47IQ8X
SEDLAVISOPROPYL ALCOHOLInstock Distributing1b31e3dc-31f3-dffe-e063-6394a90a1c962025-10-15WarningsExact identifier
unii: ND2M416302
SEDLAVISOPROPYL ALCOHOLInstock Distributing1c470960-f78d-19e7-e063-6294a90a49202025-10-15WarningsExact identifier
unii: ND2M416302
SEDLAVISOPROPYL ALCOHOLInstock Distributing1c477028-5cee-b8e2-e063-6394a90afb772025-10-15WarningsExact identifier
unii: ND2M416302
SEDLAVISOPROPYL ALCOHOLInstock Distributing1c472c35-e241-773f-e063-6294a90abb572025-10-15WarningsExact identifier
unii: ND2M416302
SEDLAVISOPROPYL ALCOHOL WIPESInstock Distributing1c478594-3118-048f-e063-6394a90a35d92025-10-15WarningsExact identifier
unii: ND2M416302
Saline AmpoulesSODIUM CHLORIDE 0.9%Trifecta Pharmaceuticals USA, LLC.ee18ef7c-bb5d-30ec-e053-2a95a90a964e2025-10-13WarningsExact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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