Asparagus Officinalis

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
6354527901
200 PELLET in 1 VIAL, GLASS (63545-279-01)
ndc11
6354527902
500 PELLET in 1 VIAL, GLASS (63545-279-02)
ndc11
6354527903
3000 PELLET in 1 BOTTLE, GLASS (63545-279-03)
ndc11
6354527904
10000 PELLET in 1 BOTTLE, GLASS (63545-279-04)

Annotations

UNII (FDA Substance ID)

Z1EJP3037Z

ASPARAGUS

RxCUI 891796

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "Z1EJP3037Z",
    "rxcui": "891796",
    "inchikey": null,
    "display_name": "ASPARAGUS",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "38621fd8-74c4-690e-e063-6294a90a72f2": {
      "match": "brand_token",
      "title": "ASPARAGUS RACEMOSUS DRY EXTRACT 40% NA (ASPARAGUS RACEMOSUS DRY EXTRACT 40%) POWDER [K. PATEL PHYTO EXTRACTIONS PRIVATE LIMITED]",
      "spl_version": "1",
      "published_date": "2025-06-27"
    }
  },
  "productid": "63545-279_bf7a265b-63b9-4289-e053-2995a90af970",
  "productndc": "63545-279",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ASPARAGUS",
  "proprietary_name": "Asparagus Officinalis",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Asparagus Officinalis",
  "start_marketing_date": "20210408",
  "active_numerator_strength": "200"
}

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