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United States · US · US:44911-0388_1bf41e20-8205-44f4-a88a-851b6c708db3

Lachesis

UNIISPL

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

Identification

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

Packs · 1

  • ndc11
    4491103881
    30 mL in 1 BOTTLE, DROPPER (44911-0388-1)

Annotations

UNII (FDA Substance ID)
VSW71SS07I
LACHESIS MUTA VENOM
RxCUI 1310458
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "VSW71SS07I",
    "rxcui": "1310458",
    "inchikey": null,
    "display_name": "LACHESIS MUTA VENOM",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "7243b1d1-b8fb-4eaf-8145-4c3bd6258765": {
      "match": "brand_token",
      "title": "LACHESIS MUTUS 7124 (LACHESIS MUTUS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "44911-0388_1bf41e20-8205-44f4-a88a-851b6c708db3",
  "productndc": "44911-0388",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LACHESIS MUTA VENOM",
  "proprietary_name": "Lachesis",
  "active_ingred_unit": "[hp_C]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Lachesis Mutus",
  "start_marketing_date": "20160822",
  "active_numerator_strength": "200"
}

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