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United States · US · US:0002-8148_65052345-9f7f-4580-8cff-1e61a421843c
HUMATROPE
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEli Lilly and Company
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1100028148011 TRAY in 1 CARTON (0002-8148-01) / 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7555-01) * 2.88 mL in 1 SYRINGE (0002-7619-01)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "INTRAMUSCULAR; SUBCUTANEOUS",
"spl_meta": {
"a774e1ae-3997-49ee-8b0e-99a2b315d409": {
"match": "brand_token",
"title": "HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY]",
"spl_version": "44",
"published_date": "2025-12-11"
}
},
"productid": "0002-8148_65052345-9f7f-4580-8cff-1e61a421843c",
"productndc": "0002-8148",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "HUMATROPE",
"active_ingred_unit": null,
"application_number": "BLA019640",
"marketing_category": "BLA",
"nonproprietary_name": "Somatropin",
"start_marketing_date": "20060127",
"active_numerator_strength": null
}Access this data programmatically
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