Formica Apis

UNIISPL

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

Identification

ManufacturerUriel Pharmacy Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4895141931
10 AMPULE in 1 BOX (48951-4193-1) / 1 mL in 1 AMPULE

Annotations

UNII (FDA Substance ID)

7S82P3R43Z

APIS MELLIFERA

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "7S82P3R43Z",
    "rxcui": null,
    "inchikey": null,
    "display_name": "APIS MELLIFERA",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "285fbafd-f390-49df-e063-6394a90a42c9": {
      "match": "brand_token",
      "title": "FORMICA APIS LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "2",
      "published_date": "2025-12-10"
    }
  },
  "productid": "48951-4193_45779954-6d64-47f6-e063-6394a90a4293",
  "productndc": "48951-4193",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "APIS MELLIFERA; FORMICA RUFA",
  "proprietary_name": "Formica Apis",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Formica Apis",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "3; 3"
}

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