BOTOX

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAllergan, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
0023392102
1 VIAL in 1 CARTON (0023-3921-02) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
ndc11
0023392103
1 VIAL in 1 CARTON (0023-3921-03) / 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": "0023-3921_7365af65-15e0-4fc1-aa6a-aaec5a43c468",
  "productndc": "0023-3921",
  "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": "20100111",
  "active_numerator_strength": "200"
}

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