Dioscorea Villosa

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
3766206321
200 PELLET in 1 VIAL, GLASS (37662-0632-1)
ndc11
3766206322
500 PELLET in 1 VIAL, GLASS (37662-0632-2)
ndc11
3766206323
3000 PELLET in 1 BOTTLE, GLASS (37662-0632-3)
ndc11
3766206324
10000 PELLET in 1 BOTTLE, GLASS (37662-0632-4)

Annotations

UNII (FDA Substance ID)

IWY3IWX2G8

DIOSCOREA VILLOSA TUBER

RxCUI 1309690

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "IWY3IWX2G8",
    "rxcui": "1309690",
    "inchikey": null,
    "display_name": "DIOSCOREA VILLOSA TUBER",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3cbcba38-218e-d4d8-e063-6394a90a1190": {
      "match": "brand_token",
      "title": "DIOSCOREA BATATA OINTMENT [URIEL PHARMACY, INC]",
      "spl_version": "1",
      "published_date": "2025-08-21"
    }
  },
  "productid": "37662-0632_e1ac85ba-a66c-ab9e-e053-2a95a90ade80",
  "productndc": "37662-0632",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DIOSCOREA VILLOSA TUBER",
  "proprietary_name": "Dioscorea Villosa",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Dioscorea Villosa",
  "start_marketing_date": "20220617",
  "active_numerator_strength": "1"
}

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