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United States · US · US:49643-017_36ad1e17-751d-e226-e063-6394a90ab328

Kapok

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
    4964301705
    5 mL in 1 VIAL, MULTI-DOSE (49643-017-05)
  • ndc11
    4964301710
    10 mL in 1 VIAL, MULTI-DOSE (49643-017-10)
  • ndc11
    4964301730
    30 mL in 1 VIAL, MULTI-DOSE (49643-017-30)
  • ndc11
    4964301750
    50 mL in 1 VIAL, MULTI-DOSE (49643-017-50)

Annotations

UNII (FDA Substance ID)
758Z9H9WV9
CEIBA PENTANDRA FIBER
RxCUI 852315
Raw payload (JSON)
{
  "unii": {
    "unii": "758Z9H9WV9",
    "rxcui": "852315",
    "inchikey": null,
    "display_name": "CEIBA PENTANDRA FIBER",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "productid": "49643-017_36ad1e17-751d-e226-e063-6394a90ab328",
  "productndc": "49643-017",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "product_type": "NON-STANDARDIZED ALLERGENIC",
  "substance_name": "CEIBA PENTANDRA FIBER",
  "proprietary_name": "Kapok",
  "active_ingred_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA",
  "nonproprietary_name": "Kapok",
  "start_marketing_date": "19740312",
  "active_numerator_strength": ".1"
}

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