Aconitum e tub. 30

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
4895113381
10 AMPULE in 1 BOX (48951-1338-1) / 1 mL in 1 AMPULE

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "ORAL",
  "spl_meta": {
    "9d04cb5d-cafa-4a64-bd6e-5724b9ee36ef": {
      "match": "brand_token",
      "title": "ACONITUM NAPELLUS 7101 (ACONITUM NAPELLUS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "48951-1338_42f33cb7-d6d8-783a-e063-6294a90a3794",
  "productndc": "48951-1338",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ACONITUM NAPELLUS",
  "proprietary_name": "Aconitum e tub. 30",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Aconitum e tub. 30",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "30"
}

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