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United States · US · US:0924-6000_f7582032-efbd-5f5b-e053-6394a90a994e
Bayer Aleve
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAcme United Corporation
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1109246000001 TABLET in 1 POUCH (0924-6000-00)
- ndc11092460000150 POUCH in 1 BOX (0924-6000-01) / 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": {
"f6f2ce71-5728-aefb-e053-6394a90a20e4": {
"match": "brand_token",
"title": "BAYER GENUINE ASPIRIN (ASPIRIN) TABLET [NAVAJO MANUFACTURING COMPANY INC.]",
"spl_version": "4",
"published_date": "2026-04-09"
}
},
"productid": "0924-6000_f7582032-efbd-5f5b-e053-6394a90a994e",
"productndc": "0924-6000",
"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": "Bayer Aleve",
"active_ingred_unit": "mg/1",
"application_number": "NDA020204",
"marketing_category": "NDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20230324",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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