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United States · US · US:85816-5106_38dfb441-b08b-b6a8-e063-6394a90a72ef

BM Digitalis Purpurea

UNIISPLATC C01AA03

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

Identification

ManufacturerBM Private Limited
CountryUS (United States)
ATC codeC01AA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    8581651061
    30000 mg in 1 BOTTLE, GLASS (85816-5106-1)

Annotations

UNII (FDA Substance ID)
F1T8QT9U8B
DIGITALIS
RxCUI 91235
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "F1T8QT9U8B",
    "rxcui": "91235",
    "inchikey": null,
    "display_name": "DIGITALIS",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "53239eb6-1403-619c-e063-6394a90a4958": {
      "match": "brand_token",
      "title": "BM NAT PHOS POTENCY (NAT PHOS) LIQUID [BM PRIVATE LIMITED]",
      "spl_version": "1",
      "published_date": "2026-06-02"
    }
  },
  "productid": "85816-5106_38dfb441-b08b-b6a8-e063-6394a90a72ef",
  "productndc": "85816-5106",
  "dosage_form": "GLOBULE",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DIGITALIS",
  "proprietary_name": "BM Digitalis Purpurea",
  "active_ingred_unit": "[hp_C]/1000mg",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Digitalis Purpurea",
  "start_marketing_date": "20150101",
  "active_numerator_strength": "30"
}

Related drugs

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