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United States · US · US:37662-2102_efd0b4af-a1b6-2e6c-e053-2995a90a70f0

Sepia

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

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
    3766221021
    200 PELLET in 1 VIAL, GLASS (37662-2102-1)
  • ndc11
    3766221022
    500 PELLET in 1 VIAL, GLASS (37662-2102-2)
  • ndc11
    3766221023
    3000 PELLET in 1 BOTTLE, GLASS (37662-2102-3)
  • ndc11
    3766221024
    10000 PELLET in 1 BOTTLE, GLASS (37662-2102-4)

Annotations

UNII (FDA Substance ID)
QDL83WN8C2
SEPIA OFFICINALIS JUICE
RxCUI 350376
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "QDL83WN8C2",
    "rxcui": "350376",
    "inchikey": null,
    "display_name": "SEPIA OFFICINALIS JUICE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "86d1f86b-db2e-0209-e053-2991aa0afec4": {
      "match": "brand_token",
      "title": "SEPIA (SEPIA OFFICINALIS JUICE\t) PELLET [BOIRON]",
      "spl_version": "4",
      "published_date": "2026-05-13"
    }
  },
  "productid": "37662-2102_efd0b4af-a1b6-2e6c-e053-2995a90a70f0",
  "productndc": "37662-2102",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SEPIA OFFICINALIS JUICE",
  "proprietary_name": "Sepia",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Sepia",
  "start_marketing_date": "20221214",
  "active_numerator_strength": "500"
}

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