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United States · US · US:85766-155_49e53ae0-1a1f-ec83-e063-6394a90a2c8d
BOTOX
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSportpharm LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1185766155011 VIAL in 1 CARTON (85766-155-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
- ndc1185766155021 VIAL in 1 CARTON (85766-155-02) / 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": "INTRADERMAL; INTRAMUSCULAR",
"spl_meta": {
"a6f42753-d31e-4b23-8da0-4b990fee4b38": {
"match": "brand_token",
"title": "BOTOX (ONABOTULINUMTOXINA) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SPORTPHARM LLC]",
"spl_version": "1",
"published_date": "2026-02-06"
}
},
"productid": "85766-155_49e53ae0-1a1f-ec83-e063-6394a90a2c8d",
"productndc": "85766-155",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BOTULINUM TOXIN TYPE A",
"proprietary_name": "BOTOX",
"active_ingred_unit": "[USP'U]/1",
"application_number": "BLA103000",
"marketing_category": "BLA",
"nonproprietary_name": "onabotulinumtoxinA",
"start_marketing_date": "19891215",
"active_numerator_strength": "100"
}Access this data programmatically
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