LMD in Sodium Chloride

UNIISPL

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

Identification

ManufacturerHospira, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0409741903
12 POUCH in 1 CASE (0409-7419-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-7419-14)

Annotations

UNII (FDA Substance ID)

K3R6ZDH4DU

DEXTRAN 40

RxCUI 3272

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "K3R6ZDH4DU",
    "rxcui": "3272",
    "inchikey": null,
    "display_name": "DEXTRAN 40",
    "substance_type": "polymer",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "3c273512-84e2-2cea-b201-12345a6bd1fe": {
      "match": "brand_token",
      "title": "LMD IN DEXTROSE (DEXTRAN 40) INJECTION, SOLUTION LMD IN SODIUM CHLORIDE (DEXTRAN 40) INJECTION, SOLUTION [HOSPIRA, INC.]",
      "spl_version": "26",
      "published_date": "2026-05-25"
    }
  },
  "productid": "0409-7419_7dc616ab-1417-4950-9e1f-2deb01b83c1a",
  "productndc": "0409-7419",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DEXTRAN 40",
  "proprietary_name": "LMD in Sodium Chloride",
  "active_ingred_unit": "g/100mL",
  "application_number": "BA720562",
  "marketing_category": "ANDA",
  "nonproprietary_name": "DEXTRAN 40",
  "start_marketing_date": "20050812",
  "active_numerator_strength": "10"
}

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