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United States · US · US:76420-766_47db098f-6da3-2339-e063-6294a90a4c84
DoubleDex Kit
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1176420766011 KIT in 1 CARTON (76420-766-01) * .9 mL in 1 PACKET (67777-419-02) * 5 mL in 1 POUCH * 25 VIAL in 1 TRAY (63323-506-01) / 1 mL in 1 VIAL
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "INTRAMUSCULAR; INTRAVENOUS; TOPICAL",
"spl_meta": {
"b7d58d9b-e1fa-4a7f-afca-beb06d028057": {
"match": "brand_token",
"title": "DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.]",
"spl_version": "9",
"published_date": "2026-01-09"
}
},
"productid": "76420-766_47db098f-6da3-2339-e063-6294a90a4c84",
"productndc": "76420-766",
"dosage_form": "KIT",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "DoubleDex Kit",
"active_ingred_unit": null,
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "Dexamethasone Sodium Phosphate, Povidine Iodine",
"start_marketing_date": "20140725",
"active_numerator_strength": null
}Access this data programmatically
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