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United States · US · US:71394-415_173eb100-b8ab-4255-bad7-466d01195c6d
LUXTURNA
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSpark Therapeutics, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1171394415011 KIT in 1 CARTON (71394-415-01) * 1 INJECTION, SUSPENSION in 1 VIAL, PLASTIC (71394-065-01) * 1 INJECTION, SOLUTION in 1 VIAL, PLASTIC (71394-716-01)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"08313a24-e7ce-457a-bb3f-161bc45517ee": {
"match": "brand_token",
"title": "LUXTURNA (VORETIGENE NEPARVOVEC-RZYL) KIT [SPARK THERAPEUTICS, INC.]",
"spl_version": "13",
"published_date": "2026-01-16"
}
},
"productid": "71394-415_173eb100-b8ab-4255-bad7-466d01195c6d",
"productndc": "71394-415",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "LUXTURNA",
"active_ingred_unit": null,
"application_number": "BLA125610",
"marketing_category": "BLA",
"nonproprietary_name": "voretigene neparvovec-rzyl",
"start_marketing_date": "20171219",
"active_numerator_strength": null
}Access this data programmatically
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