Pulsatilla Nigricans

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
3766240181
200 PELLET in 1 VIAL, GLASS (37662-4018-1)
ndc11
3766240182
500 PELLET in 1 VIAL, GLASS (37662-4018-2)
ndc11
3766240183
3000 PELLET in 1 BOTTLE, GLASS (37662-4018-3)
ndc11
3766240184
10000 PELLET in 1 BOTTLE, GLASS (37662-4018-4)

Annotations

UNII (FDA Substance ID)

8E272251DI

PULSATILLA PRATENSIS WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "8E272251DI",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PULSATILLA PRATENSIS WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "02df74e5-dcb0-4942-8c07-87faf18f145d": {
      "match": "brand_token",
      "title": "PULSATILLA 7131 (PULSATILLA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-4018_063800f4-7ae8-0e3f-e063-6294a90a537a",
  "productndc": "37662-4018",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PULSATILLA PRATENSIS WHOLE",
  "proprietary_name": "Pulsatilla Nigricans",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Pulsatilla Nigricans",
  "start_marketing_date": "20230925",
  "active_numerator_strength": "100"
}

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