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United States · US · US:0280-0130_4cd9cec2-0e06-99a3-e063-6394a90a1943
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 · 2
- ndc11028001300190 TABLET in 1 BOTTLE (0280-0130-01)
- ndc110280013002110 TABLET in 1 BOTTLE (0280-0130-02)
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": "0280-0130_4cd9cec2-0e06-99a3-e063-6394a90a1943",
"productndc": "0280-0130",
"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": "20230404",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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