Candida

UNIISPL

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

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
4964310505
5 mL in 1 VIAL, MULTI-DOSE (49643-105-05)
ndc11
4964310510
10 mL in 1 VIAL, MULTI-DOSE (49643-105-10)
ndc11
4964310530
30 mL in 1 VIAL, MULTI-DOSE (49643-105-30)
ndc11
4964310550
50 mL in 1 VIAL, MULTI-DOSE (49643-105-50)

Annotations

UNII (FDA Substance ID)

4D7G21HDBC

CANDIDA ALBICANS

RxCUI 1963

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4D7G21HDBC",
    "rxcui": "1963",
    "inchikey": null,
    "display_name": "CANDIDA ALBICANS",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "spl_meta": {
    "94dad25f-2f77-4157-ab07-87d99b06a5f0": {
      "match": "brand_token",
      "title": "CANDIDA ALB (CANDIDA ALBICANS) LIQUID [BIOACTIVE NUTRITIONAL, INC.]",
      "spl_version": "3",
      "published_date": "2026-05-20"
    }
  },
  "productid": "49643-105_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-105",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "CANDIDA ALBICANS",
  "proprietary_name": "Candida",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Candida albicans",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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