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 33 of 89 · 1,774 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ULINE Eyewash	EYEWASH	Niagara Pharmaceuticals Inc.	2d7f22d2-320b-6af1-e063-6294a90addc6	2025-11-24	Warnings	Exact identifier unii: 059QF0KO0R
Pur-Wash	EYEWASH	Niagara Pharmaceuticals, Inc.	0d43b1c1-2699-37f1-e054-00144ff88e88	2025-11-24	Warnings	Exact identifier unii: 059QF0KO0R
PUR-WASH	WATER	Niagara Pharmaceuticals Inc.	777e1559-786f-8d54-e053-2991aa0aa98d	2025-11-24	Warnings	Exact identifier unii: 059QF0KO0R
PUR-WASH	WATER	Niagara Pharmaceuticals Inc.	7289103a-5cbf-42f4-8848-e827149a43ca	2025-11-24	Warnings	Exact identifier unii: 059QF0KO0R
Natural Eyes Floaters Relief	CHELIDONIUM, EUPHRASIA, KALI SULPH, NATRUM MURIATICUM, PHOSPHORUS, PHYSOSTIGMA, SEPIA, SILICEA	TRP Company	445dc831-195e-4b25-e063-6294a90a6efd	2025-11-24	Warnings	Exact identifier unii: 451W47IQ8X
Lights Swabsticks	ISOPROPYL ALCOHOL	Lights Medical Manufacture Co., Ltd.	4435a4e6-46ae-f49b-e063-6394a90a1d9e	2025-11-22	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
CONSTIPATION	MAGNESIA CARBONICA, MAGNESIA MURIATICA, AESCULUS HIPPOCASTANUM, ALUMEN, ALUMINA, BRYONIA ALBA, NUX VOMICA, SILICEA	Natural Creations, Inc.	d2e24f5a-747b-4d62-bbdf-16c0e43becdb	2025-11-21	Warnings	Exact identifier unii: 02F3473H9O
Leuprolide Acetate	LEUPROLIDE ACETATE	VGYAAN Pharmaceuticals LLC	bec9077a-3f04-4887-856d-dde2de24584d	2025-11-21	Warnings, Adverse reactions	Exact identifier rxcui: 797544
Eyewash Additive Concentrate	WATER AND PROPYLENE GLYCOL	Haws Corporation	dd168403-398c-41ff-b1df-d93e4ff39de3	2025-11-20	Warnings	Exact identifier unii: 059QF0KO0R
MK Alcohol Prep Pads Large	ISOPROPYL ALCOHOL	Changzhou Maokang Medical Products Co., Ltd	f1ff70d7-d0f2-45db-96e9-883b54c6e441	2025-11-20	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
Vital Female Sexual Energy	AGNUS CASTUS, ARNICA MONTANA, AVENA SATIVA, CAULOPHYLLUM THALICTROIDES, CINCHONA OFFICINALIS, DAMIANA, HYPOPHYSIS SUIS, L-ARGININE, NATRUM MURIATICUM, ONOSMODIUM VIRGINIANUM, OOPHORINUM SUIS, PHOSPHORICUM ACIDUM, SEPIA, THUJA OCCIDENTALIS	Liddell Laboratories, Inc.	1ca43c82-62b0-4191-81a4-27f7f94109dd	2025-11-20	Warnings	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	Walgreen Company	d112a344-33cc-41d3-bae6-492631ebdba7	2025-11-19	Warnings	Exact identifier unii: 451W47IQ8X
Dukal Alcohol Prep Pad	ISOPROPYL ALCOHOL	Dukal LLC	953b0dd6-a667-4146-815e-6845aba0309b	2025-11-19	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
Dukal Sterile Alcohol Swabstick	ISOPROPYL ALCOHOL	Dukal LLC	8e47e9ad-cea4-76a4-e053-2a95a90ae780	2025-11-19	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
Avonex	INTERFERON BETA-1A	Biogen Inc.	d70a39cc-de15-4c12-a1ec-8063b69ea0e1	2025-11-19	Warnings, Adverse reactions	Exact identifier rxcui: 797544
Sodium chloride	SODIUM CHLORIDE	Fresenius Kabi USA, LLC	ce0c8c6f-734a-400f-9b60-a3b1e263f25f	2025-11-18	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sterile Water	WATER	Fresenius Kabi USA, LLC	fd823bef-c14c-4708-a18a-8aaa8470412f	2025-11-18	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Sodium Chloride	SODIUM CHLORIDE TABLETS	Kesin Pharma Corporation	2f107592-10c5-ef3b-e063-6394a90a7c0a	2025-11-17	Warnings	Exact identifier unii: 451W47IQ8X
Alcohol Prep Pad	ISOPROPYL ALCOHOL	Shandong Lianfa Medical Plastic Products CO.,LTD	435fd382-d2f5-b07f-e063-6294a90a7d8a	2025-11-14	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
BodyMed Alcohol Prep Pad	ALCOHOL PREP PAD	Boxout, LLC	d30dce9c-8d12-4c71-e053-2995a90a1205	2025-11-14	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

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