Berberis Vulgaris

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
6354543901
200 PELLET in 1 VIAL, GLASS (63545-439-01)
ndc11
6354543902
500 PELLET in 1 VIAL, GLASS (63545-439-02)
ndc11
6354543903
3000 PELLET in 1 BOTTLE, GLASS (63545-439-03)
ndc11
6354543904
10000 PELLET in 1 BOTTLE, GLASS (63545-439-04)

Annotations

UNII (FDA Substance ID)

1TH8Q20J0U

BERBERIS VULGARIS ROOT BARK

RxCUI 1309766

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1TH8Q20J0U",
    "rxcui": "1309766",
    "inchikey": null,
    "display_name": "BERBERIS VULGARIS ROOT BARK",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "5da48d70-1140-495d-b672-0e55c04196e1": {
      "match": "brand_token",
      "title": "BERBERIS QUARTZ LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "5",
      "published_date": "2026-01-19"
    }
  },
  "productid": "63545-439_dcb4954f-b634-890e-e053-2a95a90a304f",
  "productndc": "63545-439",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BERBERIS VULGARIS ROOT BARK",
  "proprietary_name": "Berberis Vulgaris",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Berberis Vulgaris",
  "start_marketing_date": "20220415",
  "active_numerator_strength": "100"
}

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