Scorodite Prunus

SPL

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
4895181681
10 AMPULE in 1 BOX (48951-8168-1) / 1 mL in 1 AMPULE

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "ORAL",
  "spl_meta": {
    "33bc061d-3767-4e71-b4ac-b8c8da2b0fd9": {
      "match": "brand_token",
      "title": "SCORODITE PRUNUS LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "4",
      "published_date": "2025-01-21"
    }
  },
  "productid": "48951-8168_2c28a030-bb5c-fb37-e063-6294a90aa38f",
  "productndc": "48951-8168",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BOS TAURUS PITUITARY GLAND; CAMPHOR (NATURAL); FERROUS ARSENATE; GOLD; SLOE; VERATRUM ALBUM ROOT",
  "proprietary_name": "Scorodite Prunus",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Scorodite Prunus",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "8; 4; 6; 10; 6; 4"
}

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