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United States Β· US Β· US:59088-804_463c9420-e1f4-d71d-e063-6294a90a630c
Lixofen
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPureTek Corporation
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 1
- ndc1159088804001 KIT in 1 KIT (59088-804-00) * 1 BOTTLE, DROPPER in 1 CARTON (59088-435-10) / 150 mL in 1 BOTTLE, DROPPER
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"1e2a687b-a838-9b16-e063-6394a90a69f3": {
"match": "brand_token",
"title": "LIXOFEN (DICLOFENAC SODIUM, KINESIOLOGY TAPE) KIT [PURETEK CORPORATION]",
"spl_version": "3",
"published_date": "2025-12-22"
}
},
"productid": "59088-804_463c9420-e1f4-d71d-e063-6294a90a630c",
"productndc": "59088-804",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "Lixofen",
"active_ingred_unit": null,
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "Diclofenac Sodium, kinesiology tape",
"start_marketing_date": "20240726",
"active_numerator_strength": null
}Access this data programmatically
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