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United States · US · US:68001-250_4f68e4d5-c239-eb2d-e063-6294a90af478
Zolmitriptan
Orange BookUNIISPLATC N02CC03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBluePoint Laboratories
CountryUS (United States)
ATC codeN02CC03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1168001250011 BLISTER PACK in 1 CARTON (68001-250-01) / 3 TABLET, FILM COATED in 1 BLISTER PACK (68001-250-18)
Annotations
UNII (FDA Substance ID)
2FS66TH3YW
ZOLMITRIPTAN
RxCUI 135775
Orange Book
A201779
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2FS66TH3YW",
"rxcui": "135775",
"inchikey": "ULSDMUVEXKOYBU-ZDUSSCGKSA-N",
"display_name": "ZOLMITRIPTAN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"e6628b7a-0b63-4e6f-a5e7-2fa195265235": {
"match": "brand_token",
"title": "ZOLMITRIPTAN TABLET, FILM COATED [BLUEPOINT LABORATORIES]",
"spl_version": "7",
"published_date": "2026-04-17"
}
},
"productid": "68001-250_4f68e4d5-c239-eb2d-e063-6294a90af478",
"productndc": "68001-250",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "201779",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2.5MG",
"product_no": "001",
"approval_date": "May 14, 2013"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "002",
"approval_date": "May 14, 2013"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ZOLMITRIPTAN",
"proprietary_name": "Zolmitriptan",
"active_ingred_unit": "mg/1",
"application_number": "ANDA201779",
"marketing_category": "ANDA",
"nonproprietary_name": "Zolmitriptan",
"start_marketing_date": "20140313",
"active_numerator_strength": "5"
}Related drugs
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