Eupatorium Perfoliatum

SPL

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766210001
200 PELLET in 1 VIAL, GLASS (37662-1000-1)
ndc11
3766210002
500 PELLET in 1 VIAL, GLASS (37662-1000-2)
ndc11
3766210003
3000 PELLET in 1 BOTTLE, GLASS (37662-1000-3)
ndc11
3766210004
10000 PELLET in 1 BOTTLE, GLASS (37662-1000-4)

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "ORAL",
  "spl_meta": {
    "8689017a-c21a-4b0b-9c13-9c5cde4a9148": {
      "match": "brand_token",
      "title": "EUPATORIUM PERFOLIATUM 7118 (EUPATORIUM PERFOLIATUM) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-1000_e4434837-4541-94ff-e053-2a95a90aba6b",
  "productndc": "37662-1000",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "GENTIANELLA QUINQUEFOLIA",
  "proprietary_name": "Eupatorium Perfoliatum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Eupatorium Perfoliatum",
  "start_marketing_date": "20220720",
  "active_numerator_strength": "200"
}

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