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United States · US · US:0023-1145_7365af65-15e0-4fc1-aa6a-aaec5a43c468
BOTOX
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllergan, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1100231145011 VIAL in 1 CARTON (0023-1145-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
- ndc1100231145021 VIAL in 1 CARTON (0023-1145-02) / 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": "0023-1145_7365af65-15e0-4fc1-aa6a-aaec5a43c468",
"productndc": "0023-1145",
"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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