Blatta Orientalis

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
6354550301
200 PELLET in 1 VIAL, GLASS (63545-503-01)
ndc11
6354550302
500 PELLET in 1 VIAL, GLASS (63545-503-02)
ndc11
6354550303
3000 PELLET in 1 BOTTLE, GLASS (63545-503-03)
ndc11
6354550304
10000 PELLET in 1 BOTTLE, GLASS (63545-503-04)

Annotations

UNII (FDA Substance ID)

535787266D

BLATTA ORIENTALIS

RxCUI 1346617

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "535787266D",
    "rxcui": "1346617",
    "inchikey": null,
    "display_name": "BLATTA ORIENTALIS",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "0c0490ee-23f2-1cdb-e063-6394a90a8185": {
      "match": "brand_token",
      "title": "BLATTA ORIENTALIS PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2024-01-01"
    }
  },
  "productid": "63545-503_de1fdc80-735f-9faa-e053-2995a90a59e2",
  "productndc": "63545-503",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BLATTA ORIENTALIS",
  "proprietary_name": "Blatta Orientalis",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Blatta Orientalis",
  "start_marketing_date": "20220503",
  "active_numerator_strength": "200"
}

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