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United States · US · US:15054-0500_44512f6b-6a35-4db5-ba17-fe2fe3ec5170
Dysport
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerIpsen Biopharmaceuticals, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1115054050011 VIAL in 1 CARTON (15054-0500-1) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
- ndc1115054050022 VIAL in 1 CARTON (15054-0500-2) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
- ndc1115054050091 VIAL in 1 CARTON (15054-0500-9) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Annotations
UNII (FDA Substance ID)
E211KPY694
BOTULINUM TOXIN TYPE A
RxCUI 1712
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "E211KPY694",
"rxcui": "1712",
"inchikey": null,
"display_name": "BOTULINUM TOXIN TYPE A",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAMUSCULAR",
"spl_meta": {
"71313a04-1349-4c26-b840-a39e4a3ddaed": {
"match": "brand_token",
"title": "DYSPORT (BOTULINUM TOXIN TYPE A) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GALDERMA LABORATORIES, L.P.]",
"spl_version": "12",
"published_date": "2024-10-28"
}
},
"productid": "15054-0500_44512f6b-6a35-4db5-ba17-fe2fe3ec5170",
"productndc": "15054-0500",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BOTULINUM TOXIN TYPE A",
"proprietary_name": "Dysport",
"active_ingred_unit": "U/1",
"application_number": "BLA125274",
"marketing_category": "BLA",
"nonproprietary_name": "Botulinum Toxin Type A",
"start_marketing_date": "20091102",
"active_numerator_strength": "500"
}Access this data programmatically
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