Paeonia Officinalis

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
3766219101
200 PELLET in 1 VIAL, GLASS (37662-1910-1)
ndc11
3766219102
500 PELLET in 1 VIAL, GLASS (37662-1910-2)
ndc11
3766219103
3000 PELLET in 1 BOTTLE, GLASS (37662-1910-3)
ndc11
3766219104
10000 PELLET in 1 BOTTLE, GLASS (37662-1910-4)

Annotations

UNII (FDA Substance ID)

8R564U2E1P

PAEONIA OFFICINALIS ROOT

RxCUI 1310101

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "8R564U2E1P",
    "rxcui": "1310101",
    "inchikey": null,
    "display_name": "PAEONIA OFFICINALIS ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3a9d4dc4-cd7f-586b-e063-6394a90a0eaa": {
      "match": "brand_token",
      "title": "PAEONIA OFFICINALIS (PAEONIA OFFICINALIS ROOT) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-20"
    }
  },
  "productid": "37662-1910_ed03a980-af18-59d4-e053-2995a90a583e",
  "productndc": "37662-1910",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PAEONIA OFFICINALIS ROOT",
  "proprietary_name": "Paeonia Officinalis",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Paeonia Officinalis",
  "start_marketing_date": "20221114",
  "active_numerator_strength": "1"
}

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