Drosera Rotundifolia

UNIISPL

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
3766206481
200 PELLET in 1 VIAL, GLASS (37662-0648-1)
ndc11
3766206482
500 PELLET in 1 VIAL, GLASS (37662-0648-2)
ndc11
3766206483
3000 PELLET in 1 BOTTLE, GLASS (37662-0648-3)
ndc11
3766206484
10000 PELLET in 1 BOTTLE, GLASS (37662-0648-4)

Annotations

UNII (FDA Substance ID)

QR44N9XPJQ

DROSERA ROTUNDIFOLIA WHOLE

RxCUI 283557

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "QR44N9XPJQ",
    "rxcui": "283557",
    "inchikey": null,
    "display_name": "DROSERA ROTUNDIFOLIA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "5ae94676-2b6e-4888-8691-a8aa9a6c59c9": {
      "match": "brand_token",
      "title": "DROSERA COMBINATION 9221 (DROSERA COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-0648_e1e64a61-d0eb-0f8e-e053-2a95a90af186",
  "productndc": "37662-0648",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DROSERA ROTUNDIFOLIA WHOLE",
  "proprietary_name": "Drosera Rotundifolia",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Drosera Rotundifolia",
  "start_marketing_date": "20220620",
  "active_numerator_strength": "1"
}

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