DIGITALIS PURPUREA

UNIISPLATC C01AA03

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerRxhomeo Private Limited d.b.a. Rxhomeo, Inc

CountryUS (United States)

ATC codeC01AA03

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
1563101670
100 PELLET in 1 PACKAGE (15631-0167-0)
ndc11
1563101671
200 PELLET in 1 PACKAGE (15631-0167-1)
ndc11
1563101672
400 PELLET in 1 PACKAGE (15631-0167-2)
ndc11
1563101673
750 PELLET in 1 PACKAGE (15631-0167-3)
ndc11
1563101674
2500 PELLET in 1 PACKAGE (15631-0167-4)
ndc11
1563101675
12500 PELLET in 1 PACKAGE (15631-0167-5)
ndc11
1563101676
500 PELLET in 1 PACKAGE (15631-0167-6)
ndc11
1563101677
1000 PELLET in 1 PACKAGE (15631-0167-7)

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": {
    "19ba912f-cd86-4cca-e063-6294a90a233b": {
      "match": "brand_token",
      "title": "DIGITALIS PUR LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]",
      "spl_version": "1",
      "published_date": "2024-06-03"
    }
  },
  "productid": "15631-0167_cf04f31f-424a-6c45-e053-2a95a90aa38b",
  "productndc": "15631-0167",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DIGITALIS",
  "proprietary_name": "DIGITALIS PURPUREA",
  "active_ingred_unit": "[hp_X]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "DIGITALIS PURPUREA",
  "start_marketing_date": "20151002",
  "active_numerator_strength": "6"
}

Related drugs

Other records sharing ATC code C01AA03.

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