Palmers Amaranth

UNII

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerGreer Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
2284053182
10 mL in 1 VIAL, MULTI-DOSE (22840-5318-2)
ndc11
2284053184
50 mL in 1 VIAL, MULTI-DOSE (22840-5318-4)
ndc11
2284053185
5 mL in 1 BOTTLE, DROPPER (22840-5318-5)

Annotations

UNII (FDA Substance ID)

1GH3WV23KH

AMARANTHUS PALMERI POLLEN

RxCUI 851926

Raw payload (JSON)

{
  "unii": {
    "unii": "1GH3WV23KH",
    "rxcui": "851926",
    "inchikey": null,
    "display_name": "AMARANTHUS PALMERI POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
  "productid": "22840-5318_36ac4a35-6d7b-a249-e063-6294a90a0b70",
  "productndc": "22840-5318",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "AMARANTHUS PALMERI POLLEN",
  "proprietary_name": "Palmers Amaranth",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA101833",
  "marketing_category": "BLA",
  "nonproprietary_name": "Amaranthus palmeri",
  "start_marketing_date": "19810915",
  "active_numerator_strength": ".025"
}

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