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United States · US · US:76420-264_327a22dc-b87a-2758-e063-6394a90ae257
Naproxen
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 11
- ndc1176420264011 TABLET in 1 BOTTLE (76420-264-01)
- ndc1176420264022 TABLET in 1 BOTTLE (76420-264-02)
- ndc117642026405500 TABLET in 1 BOTTLE (76420-264-05)
- ndc1176420264077 TABLET in 1 BOTTLE (76420-264-07)
- ndc117642026410100 TABLET in 1 BOTTLE (76420-264-10)
- ndc117642026412120 TABLET in 1 BOTTLE (76420-264-12)
- ndc11764202641414 TABLET in 1 BOTTLE (76420-264-14)
- ndc11764202642020 TABLET in 1 BOTTLE (76420-264-20)
- ndc11764202643030 TABLET in 1 BOTTLE (76420-264-30)
- ndc11764202646060 TABLET in 1 BOTTLE (76420-264-60)
- ndc11764202649090 TABLET in 1 BOTTLE (76420-264-90)
Annotations
UNII (FDA Substance ID)
57Y76R9ATQ
NAPROXEN
RxCUI 7258
Orange Book
A212517
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "57Y76R9ATQ",
"rxcui": "7258",
"inchikey": "CMWTZPSULFXXJA-VIFPVBQESA-N",
"display_name": "NAPROXEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c5146d73-2f34-4dfe-ac29-97071279dc4d": {
"match": "brand_token",
"title": "NAPROXEN SODIUM TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
"spl_version": "10",
"published_date": "2026-05-28"
}
},
"productid": "76420-264_327a22dc-b87a-2758-e063-6394a90ae257",
"productndc": "76420-264",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "212517",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "250MG",
"product_no": "001",
"approval_date": "Feb 21, 2020"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "375MG",
"product_no": "002",
"approval_date": "Feb 21, 2020"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "003",
"approval_date": "Feb 21, 2020"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NAPROXEN",
"proprietary_name": "Naproxen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA212517",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen",
"start_marketing_date": "20200301",
"active_numerator_strength": "500"
}Related drugs
Other records sharing ATC code G02CC02.
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