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United States · US · US:70264-011_43c866a6-dc20-5e19-e063-6294a90aac20
Aleve
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerR J General Corporation
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11702640110150 POUCH in 1 CARTON (70264-011-01) / 1 TABLET in 1 POUCH
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
N020204
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": {
"590f3be2-20df-4643-9114-e7ed4cf9155c": {
"match": "brand_token",
"title": "ALEVE (NAPROXEN SODIUM) TABLET [NAVAJO MANUFACTURING COMPANY INC.]",
"spl_version": "5",
"published_date": "2026-04-09"
}
},
"productid": "70264-011_43c866a6-dc20-5e19-e063-6294a90aac20",
"productndc": "70264-011",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "020204",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "220MG",
"product_no": "002",
"approval_date": "Jan 11, 1994"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Aleve",
"active_ingred_unit": "mg/1",
"application_number": "NDA020204",
"marketing_category": "NDA",
"nonproprietary_name": "NAPROXEN SODIUM",
"start_marketing_date": "20140226",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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