Graphites

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
3766207911
200 PELLET in 1 VIAL, GLASS (37662-0791-1)
ndc11
3766207912
500 PELLET in 1 VIAL, GLASS (37662-0791-2)
ndc11
3766207913
3000 PELLET in 1 BOTTLE, GLASS (37662-0791-3)
ndc11
3766207914
10000 PELLET in 1 BOTTLE, GLASS (37662-0791-4)

Annotations

UNII (FDA Substance ID)

4QQN74LH4O

GRAPHITE

RxCUI 90249

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4QQN74LH4O",
    "rxcui": "90249",
    "inchikey": null,
    "display_name": "GRAPHITE",
    "substance_type": "polymer",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9ca4d6aa-e183-4400-b1e0-363cb26209aa": {
      "match": "brand_token",
      "title": "GRAPHITES COMBINATION 9225 (GRAPHITES COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-0791_e3517252-4687-119c-e053-2995a90ad15a",
  "productndc": "37662-0791",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "GRAPHITE",
  "proprietary_name": "Graphites",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Graphites",
  "start_marketing_date": "20220708",
  "active_numerator_strength": "1"
}

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