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United States · US · US:0409-7418_7dc616ab-1417-4950-9e1f-2deb01b83c1a
LMD in Dextrose
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHospira, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11040974180312 POUCH in 1 CASE (0409-7418-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-7418-13)
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": "0409-7418_7dc616ab-1417-4950-9e1f-2deb01b83c1a",
"productndc": "0409-7418",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DEXTRAN 40",
"proprietary_name": "LMD in Dextrose",
"active_ingred_unit": "g/100mL",
"application_number": "BA720563",
"marketing_category": "ANDA",
"nonproprietary_name": "DEXTRAN 40",
"start_marketing_date": "20060214",
"active_numerator_strength": "10"
}Access this data programmatically
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