Ceanothus Americanus

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
3766202211
200 PELLET in 1 VIAL, GLASS (37662-0221-1)
ndc11
3766202212
500 PELLET in 1 VIAL, GLASS (37662-0221-2)
ndc11
3766202213
3000 PELLET in 1 BOTTLE, GLASS (37662-0221-3)
ndc11
3766202214
10000 PELLET in 1 BOTTLE, GLASS (37662-0221-4)

Annotations

UNII (FDA Substance ID)

25B1Y14T8N

CEANOTHUS AMERICANUS LEAF

RxCUI 1309757

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "25B1Y14T8N",
    "rxcui": "1309757",
    "inchikey": null,
    "display_name": "CEANOTHUS AMERICANUS LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "76007366-ba3c-4c7b-9dab-69306aedd57c": {
      "match": "brand_token",
      "title": "CEANOTHUS COMBINATION 9216 (CEANOTHUS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-0221_e0049d35-b615-56af-e053-2995a90ae769",
  "productndc": "37662-0221",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CEANOTHUS AMERICANUS LEAF",
  "proprietary_name": "Ceanothus Americanus",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Ceanothus Americanus",
  "start_marketing_date": "20220527",
  "active_numerator_strength": "200"
}

Access this data programmatically

Query Ceanothus Americanus and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs