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United States · US · US:49643-011_36ad1e17-751d-e226-e063-6394a90ab328

Goat Epithelia

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAllermed Laboratories, Inc.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    4964301105
    5 mL in 1 VIAL, MULTI-DOSE (49643-011-05)
  • ndc11
    4964301110
    10 mL in 1 VIAL, MULTI-DOSE (49643-011-10)
  • ndc11
    4964301130
    30 mL in 1 VIAL, MULTI-DOSE (49643-011-30)
  • ndc11
    4964301150
    50 mL in 1 VIAL, MULTI-DOSE (49643-011-50)

Annotations

UNII (FDA Substance ID)
JLG9853E2P
CAPRA HIRCUS SKIN
RxCUI 852252
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "JLG9853E2P",
    "rxcui": "852252",
    "inchikey": null,
    "display_name": "CAPRA HIRCUS SKIN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "8d2cb3f8-52d3-473e-ae8b-1da97bea8dba": {
      "match": "brand_token",
      "title": "GOAT DEWORMER (FENBENDAZOLE) SUSPENSION [PET PROFESSIONAL INC.]",
      "spl_version": "1",
      "published_date": "2025-12-02"
    }
  },
  "productid": "49643-011_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-011",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "CAPRA HIRCUS SKIN",
  "proprietary_name": "Goat Epithelia",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Goat Epithelia",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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