Folixate

UNIISPL

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

Identification

ManufacturerPureTek Corporation

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5908830154
30 TABLET in 1 BOTTLE, PLASTIC (59088-301-54)

Annotations

UNII (FDA Substance ID)

A9R10K3F2F

LEVOMEFOLATE CALCIUM

RxCUI 1028454

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "A9R10K3F2F",
    "rxcui": "1028454",
    "inchikey": "VWBBRFHSPXRJQD-QNTKWALQSA-L",
    "display_name": "LEVOMEFOLATE CALCIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "0bb91f61-b61b-c894-e063-6394a90ae51c": {
      "match": "brand_token",
      "title": "FOLIXATE (FOLATE, VITAMIN D3) TABLET [PURETEK CORPORATION]",
      "spl_version": "1",
      "published_date": "2023-12-07"
    }
  },
  "productid": "59088-301_0bb91f61-b61a-c894-e063-6394a90ae51c",
  "productndc": "59088-301",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LEVOMEFOLATE CALCIUM; VITAMIN D",
  "proprietary_name": "Folixate",
  "active_ingred_unit": "ug/1; ug/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Folate, Vitamin D3",
  "start_marketing_date": "20231205",
  "active_numerator_strength": "1000; 125"
}

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