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United States · US · US:49643-326_36ad1e17-751d-e226-e063-6394a90ab328

Grama grass Pollen

UNII

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAllermed Laboratories, Inc.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    4964332605
    5 mL in 1 VIAL, MULTI-DOSE (49643-326-05)
  • ndc11
    4964332610
    10 mL in 1 VIAL, MULTI-DOSE (49643-326-10)
  • ndc11
    4964332630
    30 mL in 1 VIAL, MULTI-DOSE (49643-326-30)
  • ndc11
    4964332650
    50 mL in 1 VIAL, MULTI-DOSE (49643-326-50)

Annotations

UNII (FDA Substance ID)
2XO08315X1
BOUTELOUA GRACILIS POLLEN
Raw payload (JSON)
{
  "unii": {
    "unii": "2XO08315X1",
    "rxcui": null,
    "inchikey": null,
    "display_name": "BOUTELOUA GRACILIS POLLEN",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-326_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-326",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "BOUTELOUA GRACILIS POLLEN",
  "proprietary_name": "Grama grass Pollen",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Bouteloua spp.",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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