Ruta Graveolens

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 · 3

ndc11
3766222611
200 PELLET in 1 VIAL, GLASS (37662-2261-1)
ndc11
3766222612
1200 PELLET in 1 BOTTLE, GLASS (37662-2261-2)
ndc11
3766222613
4000 PELLET in 1 BOTTLE, GLASS (37662-2261-3)

Annotations

UNII (FDA Substance ID)

N94C2U587S

RUTA GRAVEOLENS FLOWERING TOP

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "N94C2U587S",
    "rxcui": null,
    "inchikey": null,
    "display_name": "RUTA GRAVEOLENS FLOWERING TOP",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "dd101fac-fa41-40b0-81cb-32fb79247403": {
      "match": "brand_token",
      "title": "RUTA GRAVEOLENS 7133 (RUTA GRAVEOLENS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-2261_f1a3bd93-80d5-be37-e053-2a95a90a3fd9",
  "productndc": "37662-2261",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "RUTA GRAVEOLENS FLOWERING TOP",
  "proprietary_name": "Ruta Graveolens",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Ruta Graveolens",
  "start_marketing_date": "20230106",
  "active_numerator_strength": "6"
}

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