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United States · US · US:49643-010_36ad1e17-751d-e226-e063-6394a90ab328

Flaxseed

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
    4964301005
    5 mL in 1 VIAL, MULTI-DOSE (49643-010-05)
  • ndc11
    4964301010
    10 mL in 1 VIAL, MULTI-DOSE (49643-010-10)
  • ndc11
    4964301030
    30 mL in 1 VIAL, MULTI-DOSE (49643-010-30)
  • ndc11
    4964301050
    50 mL in 1 VIAL, MULTI-DOSE (49643-010-50)

Annotations

UNII (FDA Substance ID)
4110YT348C
FLAX SEED
RxCUI 318224
Raw payload (JSON)
{
  "unii": {
    "unii": "4110YT348C",
    "rxcui": "318224",
    "inchikey": null,
    "display_name": "FLAX SEED",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-010_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-010",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "FLAX SEED",
  "proprietary_name": "Flaxseed",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Flaxseed",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".05"
}

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