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 10 of 90 · 1,798 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
leuprolide acetateLEUPROLIDE ACETATEAmneal Pharmaceuticals LLC4838c674-044e-46b2-81e7-c691b99d8fa52026-05-28Warnings, Adverse reactionsExact identifier
rxcui: 797544
PlegisolPOTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, AND MAGNESIUM CHLORIDEHospira, Inc.35a174f0-f0d7-4ec7-3f81-d3d572c059cf2026-05-27Warnings, Adverse reactionsExact identifier
unii: 02F3473H9O
unii: 451W47IQ8X
THAMTROMETHAMINEHospira, Inc.4af52118-c12b-4ad5-30bb-959848357e8a2026-05-27Warnings, Adverse reactionsExact identifier
unii: 023C2WHX2V
MyMedic Sting Relief WipeBENZOCAINE, ISOPROPYL ALCOHOLChangzhou Maokang Medical Products Co., Ltd52b5653e-289c-d99e-e063-6294a90aa6472026-05-26WarningsExact identifier
unii: ND2M416302
TPN ElectrolytesSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, AND SODIUM ACETATE ANHYDROUSHospira, Inc.c00817bc-7b62-4abe-0280-e7930eda3f942026-05-25Warnings, Adverse reactionsExact identifier
unii: 02F3473H9O
unii: 451W47IQ8X
LEUPROLIDE ACETATELEUPROLIDE ACETATEZydus Pharmaceuticals USA Inc.35634415-000f-47db-9bd7-9e16eef3f02e2026-05-25Warnings, Adverse reactionsExact identifier
rxcui: 797544
Swab Applicator Brushes 8.3% w/w Povidone-Iodine and 72.5% w/w Isopropyl Alcohol (IPA)POVIDONE-IODINE, ISOPROPYL ALCOHOLXINXIANG XINDA TECHNOLOGY CO.,LTD529b8ad6-081e-0ef8-e063-6294a90a67df2026-05-24WarningsExact identifier
unii: ND2M416302
Swab Stick 2% w/w chlorhexidine gluconate (CHG) and 70% v/v isopropyI alcohol (IPA)CHLORHEXIDINE GLUCONATE, ISOPROPYI ALCOHOLXINXIANG XINDA TECHNOLOGY CO.,LTD51c42761-3a7a-172d-e063-6394a90a53332026-05-24WarningsExact identifier
unii: ND2M416302
Bacteriostatic WaterBACTERIOSTATIC WATERHospira, Inc.87d6e9dc-fe3b-4593-ac9a-d7493d1959c72026-05-22Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
CyltezoADALIMUMAB-ADBMBoehringer Ingelheim Pharmaceuticals, Inc.115ea79b-7209-7f19-b35d-36ec0828fbf52026-05-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 797544
SALINE CLEANINGSODIUM CHLORIDEGuangzhou Huanmei Cosmetics Co., Ltd.524f07cc-ddb9-dda5-e063-6394a90ac0a52026-05-21WarningsExact identifier
unii: 451W47IQ8X
Walgreens 70% Isopropyl Alcohol WipesISOPROPYL ALCOHOLWalgreen Companye8b0ecc3-3a30-47c9-b7d1-518681d575b42026-05-21WarningsExact identifier
rxcui: 797544
unii: ND2M416302
70% Isopropyl Alcohol70% ISOPROPYL ALCOHOLGreatdealson, Inc.4aa809cd-500a-dd65-e063-6394a90a31442026-05-20Warnings, Adverse reactionsExact identifier
unii: ND2M416302
WHITENING SUNSCREENANTI WRINKLEWHITENING SUNSCREENANTI WRINKLEShantou Oushiya Biotechnology Co.,Ltd524384e9-b3f8-4c13-e063-6394a90a89732026-05-20WarningsExact identifier
unii: 059QF0KO0R
Sodium ChlorideSODIUM CHLORIDEHospira, Inc.a2a964f7-c3ec-4dfb-e3a0-6d8136a803972026-05-19Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
CVS Isopropyl Rubbing Alcohol WipesISOPROPYL ALCOHOLCVS PHARMACY, INC7e027210-9729-4659-8a75-b6b2ac60f7bc2026-05-19WarningsExact identifier
rxcui: 797544
unii: ND2M416302
CVS Isopropyl Rubbing Alcohol PadsISOPROPYL ALCOHOLCVS PHARMACY, INCe65b3363-71d9-47b6-a044-edac18f9858f2026-05-19WarningsExact identifier
rxcui: 797544
unii: ND2M416302
Leuprolide AcetateLEUPROLIDE ACETATESandoz Inc8bd72c1e-2751-4498-a346-bc5e3acbba0b2026-05-19Warnings, Adverse reactionsExact identifier
rxcui: 797544
Wish Alcohol PadISOPROPYL ALCOHOL CLOTHYiwu Ori-Power Medtech Co.,Ltd.51f87ed7-04ae-136a-e063-6294a90a95002026-05-16WarningsExact identifier
rxcui: 797544
unii: ND2M416302
Alcohol prep padISOPROPYL ALCOHOL CLOTHHubei V-Medical Products co.,Ltd.51d5780e-9039-1b66-e063-6394a90a0b8a2026-05-15WarningsExact identifier
rxcui: 797544
unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

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