Anticoagulant Citrate Dextrose A

UNIISPL

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

Identification

ManufacturerCitra Labs LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
2373160511
10 VIAL, SINGLE-USE in 1 CASE (23731-6051-1) / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)
ndc11
2373160512
25 VIAL, SINGLE-USE in 1 CASE (23731-6051-2) / 30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)
ndc11
2373160513
30 mL in 1 VIAL, SINGLE-USE (23731-6051-3)

Annotations

UNII (FDA Substance ID)

XF417D3PSL

ANHYDROUS CITRIC ACID

RxCUI 221946

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "XF417D3PSL",
    "rxcui": "221946",
    "inchikey": "KRKNYBCHXYNGOX-UHFFFAOYSA-N",
    "display_name": "ANHYDROUS CITRIC ACID",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "EXTRACORPOREAL",
  "spl_meta": {
    "db8334be-5b8b-4811-811a-efbe32b6d147": {
      "match": "brand_token",
      "title": "ANTICOAGULANT SODIUM CITRATE (TRISODIUM CITRATE DIHYDRATE) SOLUTION [LABORATORIOS GRIFOLS SA]",
      "spl_version": "7",
      "published_date": "2026-04-20"
    }
  },
  "productid": "23731-6051_9a133b17-0377-431f-b839-3e090fdabd78",
  "productndc": "23731-6051",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE",
  "proprietary_name": "Anticoagulant Citrate Dextrose A",
  "active_ingred_unit": "g/10mL; g/10mL; g/10mL",
  "application_number": "BN020037",
  "marketing_category": "NDA",
  "nonproprietary_name": "Anhydrous Citric Acid, Dextrose Monohydrate, and Trisodium Citrate Dihydrate",
  "start_marketing_date": "20030826",
  "active_numerator_strength": ".073; .245; .22"
}

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