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United States · US · US:0591-2533_f2d33c82-a69f-4f6a-bd74-2c91efd6cab8
Dalfampridine
Orange BookUNIISPLATC N07XX07
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerActavis Pharma, Inc.
CountryUS (United States)
ATC codeN07XX07
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11059125336060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-2533-60)
Annotations
UNII (FDA Substance ID)
BH3B64OKL9
DALFAMPRIDINE
RxCUI 897018
Orange Book
A206836
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "BH3B64OKL9",
"rxcui": "897018",
"inchikey": "NUKYPUAOHBNCPY-UHFFFAOYSA-N",
"display_name": "DALFAMPRIDINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"354a97e8-35c8-418b-91b2-9e8e066cec65": {
"match": "brand_token",
"title": "DALFAMPRIDINE TABLET, FILM COATED, EXTENDED RELEASE [ACCORD HEALTHCARE INC.]",
"spl_version": "8",
"published_date": "2025-11-17"
}
},
"productid": "0591-2533_f2d33c82-a69f-4f6a-bd74-2c91efd6cab8",
"productndc": "0591-2533",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "206836",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "001",
"approval_date": "Jan 23, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DALFAMPRIDINE",
"proprietary_name": "Dalfampridine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA206836",
"marketing_category": "ANDA",
"nonproprietary_name": "Dalfampridine",
"start_marketing_date": "20220531",
"active_numerator_strength": "10"
}Related drugs
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