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United States · US · US:65862-626_b813e372-4315-4a35-a6dd-592b69aee7b8
Rizatriptan Benzoate
Orange BookUNIISPLATC N02CC04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAurobindo Pharma Limited
CountryUS (United States)
ATC codeN02CC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc1165862626124 BLISTER PACK in 1 CARTON (65862-626-12) / 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-626-03)
- ndc1165862626183 BLISTER PACK in 1 CARTON (65862-626-18) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-626-06)
- ndc1165862626369 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65862-626-36)
- ndc11658626264818 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65862-626-48)
- ndc1165862626641 BLISTER PACK in 1 CARTON (65862-626-64) / 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-626-03)
- ndc1165862626903 BLISTER PACK in 1 CARTON (65862-626-90) / 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-626-03)
Annotations
UNII (FDA Substance ID)
WR978S7QHH
RIZATRIPTAN BENZOATE
RxCUI 237082
Orange Book
A203062
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WR978S7QHH",
"rxcui": "237082",
"inchikey": "JPRXYLQNJJVCMZ-UHFFFAOYSA-N",
"display_name": "RIZATRIPTAN BENZOATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"f754388d-77f1-0d8d-e053-6394a90a7b7e": {
"match": "brand_token",
"title": "RIZATRIPTAN BENZOATE TABLET, FILM COATED [DIRECT_RX]",
"spl_version": "4",
"published_date": "2026-03-18"
}
},
"productid": "65862-626_b813e372-4315-4a35-a6dd-592b69aee7b8",
"productndc": "65862-626",
"dosage_form": "TABLET, ORALLY DISINTEGRATING",
"orange_book": {
"appl_no": "203062",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 5MG BASE",
"product_no": "001",
"approval_date": "Jul 1, 2013"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 10MG BASE",
"product_no": "002",
"approval_date": "Jul 1, 2013"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RIZATRIPTAN BENZOATE",
"proprietary_name": "Rizatriptan Benzoate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA203062",
"marketing_category": "ANDA",
"nonproprietary_name": "Rizatriptan Benzoate",
"start_marketing_date": "20130701",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code N02CC04.
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