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United States · US · US:69452-341_4dcbf4e0-a9ed-44d9-b610-024173094971
Naratriptan
Orange BookUNIISPLATC N02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBionpharma Inc.
CountryUS (United States)
ATC codeN02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1169452341721 BLISTER PACK in 1 CARTON (69452-341-72) / 9 TABLET, FILM COATED in 1 BLISTER PACK (69452-341-60)
Annotations
UNII (FDA Substance ID)
10X8X4P12Z
NARATRIPTAN HYDROCHLORIDE
RxCUI 236690
Orange Book
A091441
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": "69452-341_4dcbf4e0-a9ed-44d9-b610-024173094971",
"productndc": "69452-341",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "091441",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 1MG BASE",
"product_no": "001",
"approval_date": "Apr 30, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 2.5MG BASE",
"product_no": "002",
"approval_date": "Apr 30, 2012"
}
],
"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": "ANDA091441",
"marketing_category": "ANDA",
"nonproprietary_name": "Naratriptan",
"start_marketing_date": "20220411",
"active_numerator_strength": "2.5"
}Related drugs
Other records sharing ATC code N02CC02.
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