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United States · US · US:71335-1869_3f020a02-71fd-4194-abac-d29da8af014b
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 · 8
- ndc11713351869130 TABLET in 1 BOTTLE (71335-1869-1)
- ndc11713351869260 TABLET in 1 BOTTLE (71335-1869-2)
- ndc11713351869320 TABLET in 1 BOTTLE (71335-1869-3)
- ndc117133518694120 TABLET in 1 BOTTLE (71335-1869-4)
- ndc11713351869510 TABLET in 1 BOTTLE (71335-1869-5)
- ndc11713351869690 TABLET in 1 BOTTLE (71335-1869-6)
- ndc11713351869740 TABLET in 1 BOTTLE (71335-1869-7)
- ndc11713351869845 TABLET in 1 BOTTLE (71335-1869-8)
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": "71335-1869_3f020a02-71fd-4194-abac-d29da8af014b",
"productndc": "71335-1869",
"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": "250"
}Related drugs
Other records sharing ATC code G02CC02.
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