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United States · US · US:71335-2777_7218d46c-3db2-4c6e-8b5b-58b8d576d4d0
Naproxen
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 10
- ndc11713352777028 TABLET in 1 BOTTLE (71335-2777-0)
- ndc11713352777130 TABLET in 1 BOTTLE (71335-2777-1)
- ndc11713352777260 TABLET in 1 BOTTLE (71335-2777-2)
- ndc11713352777310 TABLET in 1 BOTTLE (71335-2777-3)
- ndc11713352777490 TABLET in 1 BOTTLE (71335-2777-4)
- ndc11713352777520 TABLET in 1 BOTTLE (71335-2777-5)
- ndc117133527776120 TABLET in 1 BOTTLE (71335-2777-6)
- ndc11713352777714 TABLET in 1 BOTTLE (71335-2777-7)
- ndc11713352777842 TABLET in 1 BOTTLE (71335-2777-8)
- ndc11713352777940 TABLET in 1 BOTTLE (71335-2777-9)
Annotations
UNII (FDA Substance ID)
57Y76R9ATQ
NAPROXEN
RxCUI 7258
Orange Book
A200429
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": "71335-2777_7218d46c-3db2-4c6e-8b5b-58b8d576d4d0",
"productndc": "71335-2777",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "200429",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "250MG",
"product_no": "001",
"approval_date": "Nov 8, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "375MG",
"product_no": "002",
"approval_date": "Nov 8, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "003",
"approval_date": "Nov 8, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NAPROXEN",
"proprietary_name": "Naproxen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA200429",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen",
"start_marketing_date": "20111108",
"active_numerator_strength": "500"
}Related drugs
Other records sharing ATC code G02CC02.
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