Indigo

UNII

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 · 1

ndc11
3766236951
10000 PELLET in 1 BOTTLE, PLASTIC (37662-3695-1)

Annotations

UNII (FDA Substance ID)

1G5BK41P4F

INDIGO

RxCUI 1426889

Raw payload (JSON)

{
  "unii": {
    "unii": "1G5BK41P4F",
    "rxcui": "1426889",
    "inchikey": "COHYTHOBJLSHDF-BUHFOSPRSA-N",
    "display_name": "INDIGO",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "37662-3695_021103af-6167-d747-e063-6394a90a9b4e",
  "productndc": "37662-3695",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "INDIGO",
  "proprietary_name": "Indigo",
  "active_ingred_unit": "[hp_Q]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Indigo",
  "start_marketing_date": "20230803",
  "active_numerator_strength": "1"
}

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