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United States · US · US:58394-015_5f2d1c61-a588-484c-b240-3bf0e6120713
Xyntha
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWyeth BioPharma Division of Wyeth Pharmaceuticals LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1158394015011 KIT in 1 CARTON (58394-015-01) * 1 mL in 1 PACKET * 4 mL in 1 VIAL, SINGLE-USE (58394-115-01) * 4 mL in 1 SYRINGE (58394-018-01)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"25ea1c3c-14a2-ef11-302e-012bd683924f": {
"match": "brand_token",
"title": "XYNTHA (ANTIHEMOPHILIC FACTOR (RECOMBINANT)) KIT [WYETH BIOPHARMA DIVISION OF WYETH PHARMACEUTICALS LLC]",
"spl_version": "35",
"published_date": "2026-03-20"
}
},
"productid": "58394-015_5f2d1c61-a588-484c-b240-3bf0e6120713",
"productndc": "58394-015",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "PLASMA DERIVATIVE",
"substance_name": null,
"proprietary_name": "Xyntha",
"active_ingred_unit": null,
"application_number": "BLA125264",
"marketing_category": "BLA",
"nonproprietary_name": "antihemophilic factor (recombinant)",
"start_marketing_date": "20080801",
"active_numerator_strength": null
}Access this data programmatically
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