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United States · US · US:0280-6010_4526b265-424f-3e71-e063-6294a90a21a8
Aleve
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBayer HealthCare LLC.
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 11
- ndc1102806010011 BOTTLE in 1 CARTON (0280-6010-01) / 100 TABLET in 1 BOTTLE
- ndc1102806010021 BOTTLE in 1 CARTON (0280-6010-02) / 130 TABLET in 1 BOTTLE
- ndc1102806010031 BOTTLE in 1 CARTON (0280-6010-03) / 150 TABLET in 1 BOTTLE
- ndc1102806010041 BOTTLE in 1 CARTON (0280-6010-04) / 36 TABLET in 1 BOTTLE
- ndc1102806010051 BOTTLE in 1 CARTON (0280-6010-05) / 65 TABLET in 1 BOTTLE
- ndc110280601006225 TABLET in 1 BOTTLE (0280-6010-06)
- ndc110280601007270 TABLET in 1 BOTTLE (0280-6010-07)
- ndc11028060100990 TABLET in 1 BOTTLE (0280-6010-09)
- ndc1102806010101 BOTTLE in 1 TRAY (0280-6010-10) / 10 TABLET in 1 BOTTLE
- ndc1102806010241 BOTTLE in 1 CARTON (0280-6010-24) / 24 TABLET in 1 BOTTLE
- ndc1102806010501 BOTTLE in 1 CARTON (0280-6010-50) / 50 TABLET in 1 BOTTLE
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": "0280-6010_4526b265-424f-3e71-e063-6294a90a21a8",
"productndc": "0280-6010",
"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": "20020726",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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