🇺🇸
United States · US · US:44183-850_e0a82608-7b67-4d15-a04a-16e6c341c621
Sumatriptan Succinate and Naproxen Sodium
Orange BookUNIISPLATC G02CC
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCurrax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven
CountryUS (United States)
ATC codeG02CC
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1144183850099 TABLET in 1 BOTTLE (44183-850-09)
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
N021926
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9TN87S3A3C",
"rxcui": "142442",
"inchikey": "CDBRNDSHEYLDJV-FVGYRXGTSA-M",
"display_name": "NAPROXEN SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"65147b04-0b6b-4d30-9710-d5cdce85e8f5": {
"match": "brand_token",
"title": "SUMATRIPTAN INJECTION, SOLUTION [ARMAS PHARMACEUTICALS INC.]",
"spl_version": "2",
"published_date": "2026-06-02"
}
},
"productid": "44183-850_e0a82608-7b67-4d15-a04a-16e6c341c621",
"productndc": "44183-850",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "021926",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "500MG;EQ 85MG BASE",
"product_no": "001",
"approval_date": "Apr 15, 2008"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "60MG;EQ 10MG BASE",
"product_no": "002",
"approval_date": "May 14, 2015"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE",
"proprietary_name": "Sumatriptan Succinate and Naproxen Sodium",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "NDA021926",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "sumatriptan succinate and naproxen sodium",
"start_marketing_date": "20150514",
"active_numerator_strength": "500; 85"
}Related drugs
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