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United States · US · US:0054-0278_14eeba7d-700d-4ac1-a71e-d6a1fca8aaab
Naratriptan
Orange BookUNIISPLATC N02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHikma Pharmaceuticals USA Inc.
CountryUS (United States)
ATC codeN02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1100540278039 TABLET in 1 BOTTLE (0054-0278-03)
Annotations
UNII (FDA Substance ID)
10X8X4P12Z
NARATRIPTAN HYDROCHLORIDE
RxCUI 236690
Orange Book
A090381
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "10X8X4P12Z",
"rxcui": "236690",
"inchikey": "AWEZYKMQFAUBTD-UHFFFAOYSA-N",
"display_name": "NARATRIPTAN HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"41c29652-32f8-48dc-9038-0e2195aa2084": {
"match": "brand_token",
"title": "NARATRIPTAN TABLET [HERITAGE PHARMACEUTICALS INC. D/B/A AVET PHARMACEUTICALS INC.]",
"spl_version": "20",
"published_date": "2025-11-17"
}
},
"productid": "0054-0278_14eeba7d-700d-4ac1-a71e-d6a1fca8aaab",
"productndc": "0054-0278",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "090381",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 1MG BASE",
"product_no": "001",
"approval_date": "Jul 7, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 2.5MG BASE",
"product_no": "002",
"approval_date": "Jul 7, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NARATRIPTAN HYDROCHLORIDE",
"proprietary_name": "Naratriptan",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090381",
"marketing_category": "ANDA",
"nonproprietary_name": "Naratriptan",
"start_marketing_date": "20100707",
"active_numerator_strength": "1"
}Related drugs
Other records sharing ATC code N02CC02.
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