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 22 of 89 · 1,774 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Isopropyl AlcoholISOPROPYL ALCOHOLCariba International001c1fcf-2808-467c-86d8-c038513fa3b52026-01-29WarningsExact identifier
unii: ND2M416302
70%ISOPROPYL ALCOHOLCariba International483586f4-aab4-40c2-8925-c4f7fb22c6aa2026-01-29Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Singular Wipes UnscentedISOPROPYL ALCOHOLSINGULAR ENTERPRISES LLCac2b352f-6cb2-4683-bb41-13e8ecb186bf2026-01-27WarningsExact identifier
rxcui: 797544
unii: ND2M416302
Sodium ChlorideSODIUM CHLORIDENephron Pharmaceuticals Corporationa4edf2d5-a9ff-30d4-e053-2995a90a56502026-01-26Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Everlit Survival Sting Relief PadISOPROPYL ALCOHOLEVERLIT GLOBAL INC.3a0414ea-f862-aa0f-e063-6294a90aecb72026-01-23WarningsExact identifier
unii: ND2M416302
EVERLIT SURVIVAL PREP PADISOPROPYL ALCOHOLEVERLIT GLOBAL INC.3a03ed81-5b1d-172e-e063-6394a90ac59c2026-01-23WarningsExact identifier
rxcui: 797544
unii: ND2M416302
Rite Aid Isopropyl Alcohol WipesISOPROPYL ALCOHOLRite Aidbca837b0-5044-4e97-e053-2a95a90a13af2026-01-22WarningsExact identifier
rxcui: 797544
unii: ND2M416302
Lights Isopropyl Alcohol Prep PadsISOPROPYL ALCOHOLLights Medical Manufacture Co., Ltd.4905a27c-6cf8-4b1a-a02c-4c81756e8c0a2026-01-21WarningsExact identifier
rxcui: 797544
unii: ND2M416302
LIGHTS Instant Sting Relief PadBENZOCAINELights Medical Manufacture Co., Ltd.28dd82a7-f360-a022-e063-6394a90a3a762026-01-21WarningsExact identifier
unii: ND2M416302
DOP Isopropyl Rubbing Alcohol 70%ISOPROPYL ALCOHOLOmega & Delta Co., Inc.c779a35b-1118-4560-8d77-6878edb4c2672026-01-21WarningsExact identifier
unii: ND2M416302
INSULIN DILUTING MEDIUM FOR KirstyWATERBiocon Biologics Inc.3db1d482-7e1f-aec6-79ef-3f305b4d82772026-01-20Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Sodium ChlorideSODIUM CHLORIDEProPharma Distribution48d73434-e65b-dc98-e063-6294a90affa22026-01-20Adverse reactionsExact identifier
unii: 451W47IQ8X
Equate Comfort Flow Sinus washSINUS WASHWALMART INC9e911eef-ca99-9902-e053-2a95a90aab0e2026-01-19WarningsExact identifier
unii: 451W47IQ8X
EQUATE PREMIUM SALINESODIUM CHLORIDE 0.65%Walmart Stores, Inc.1e17f022-f513-140d-e063-6394a90a379e2026-01-19WarningsExact identifier
unii: 451W47IQ8X
Sodium chlorideSODIUM CHLORIDEFresenius Kabi USA, LLCd98bf9f7-30ec-4927-a577-cabad192cb182026-01-19Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Adalimumab-ryvkADALIMUMAB-RYVKQuallent Pharmaceuticals Health LLCdce1590f-9e47-4c4d-9437-cfb18b779a752026-01-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 797544
NEXXGEN 50% RUBBING ALCOHOLISOPROPYL ALCOHOLA & A Nexxgen LLCd48232ab-ab55-488a-9cc1-77c8d0ba992e2026-01-16WarningsExact identifier
unii: ND2M416302
leuprolide acetateLEUPROLIDE ACETATEPAI Holdings, LLC dba PAI Pharma19be0b7f-e68a-4547-9e49-b51b128219072026-01-16Warnings, Adverse reactionsExact identifier
rxcui: 797544
Sodium Chloride HypertonicitySODIUM CHLORIDECVS Pharmacy9245d842-7f78-42d8-83ba-8eb9ec8dbc0d2026-01-15WarningsExact identifier
unii: 451W47IQ8X
Sodium Chloride HypertonicitySODIUM CHLORIDECVS PHARMACYd5cc6cd1-ddf8-4f5b-a021-204cdda0db942026-01-15WarningsExact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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