Angustura Vera

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
6354500701
200 PELLET in 1 VIAL, GLASS (63545-007-01)
ndc11
6354500702
500 PELLET in 1 VIAL, GLASS (63545-007-02)
ndc11
6354500703
3000 PELLET in 1 BOTTLE, GLASS (63545-007-03)
ndc11
6354500704
10000 PELLET in 1 BOTTLE, GLASS (63545-007-04)

Annotations

UNII (FDA Substance ID)

104010O5VU

ANGOSTURA BARK

RxCUI 1322552

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "104010O5VU",
    "rxcui": "1322552",
    "inchikey": null,
    "display_name": "ANGOSTURA BARK",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "b714db67-0739-0c80-e053-2995a90a5079": {
      "match": "brand_token",
      "title": "ANGUSTURA VERA PELLET [HAHNEMANN LABORATORIES, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-13"
    }
  },
  "productid": "63545-007_2b48f9da-cad7-61ce-e063-6394a90a01d0",
  "productndc": "63545-007",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ANGOSTURA BARK",
  "proprietary_name": "Angustura Vera",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Angustura Vera",
  "start_marketing_date": "20201222",
  "active_numerator_strength": "1"
}

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