Cocculus Indicus

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
3766204671
80 PELLET in 1 VIAL, GLASS (37662-0467-1)
ndc11
3766204672
200 PELLET in 1 VIAL, GLASS (37662-0467-2)
ndc11
3766204673
1200 PELLET in 1 BOTTLE, GLASS (37662-0467-3)
ndc11
3766204674
4000 PELLET in 1 BOTTLE, GLASS (37662-0467-4)

Annotations

UNII (FDA Substance ID)

810258W28U

ANAMIRTA COCCULUS SEED

RxCUI 1310018

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "810258W28U",
    "rxcui": "1310018",
    "inchikey": null,
    "display_name": "ANAMIRTA COCCULUS SEED",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "852e9d96-bc27-1dd8-e053-2991aa0abba5": {
      "match": "brand_token",
      "title": "COCCULUS INDICUS (ANAMIRTA COCCULUS SEED\t) PELLET [BOIRON]",
      "spl_version": "3",
      "published_date": "2026-05-13"
    }
  },
  "productid": "37662-0467_e11d2015-acb5-5f6d-e053-2a95a90a891a",
  "productndc": "37662-0467",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ANAMIRTA COCCULUS SEED",
  "proprietary_name": "Cocculus Indicus",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Cocculus Indicus",
  "start_marketing_date": "20220610",
  "active_numerator_strength": "30"
}

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