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United States · US · US:71335-0822_25e161db-5f02-4458-bec7-b5a99f425a19
Naproxen Sodium
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
- ndc1171335082206 TABLET, FILM COATED in 1 BOTTLE (71335-0822-0)
- ndc11713350822120 TABLET, FILM COATED in 1 BOTTLE (71335-0822-1)
- ndc117133508222100 TABLET, FILM COATED in 1 BOTTLE (71335-0822-2)
- ndc11713350822330 TABLET, FILM COATED in 1 BOTTLE (71335-0822-3)
- ndc117133508224120 TABLET, FILM COATED in 1 BOTTLE (71335-0822-4)
- ndc11713350822560 TABLET, FILM COATED in 1 BOTTLE (71335-0822-5)
- ndc11713350822690 TABLET, FILM COATED in 1 BOTTLE (71335-0822-6)
- ndc11713350822742 TABLET, FILM COATED in 1 BOTTLE (71335-0822-7)
- ndc11713350822814 TABLET, FILM COATED in 1 BOTTLE (71335-0822-8)
- ndc11713350822956 TABLET, FILM COATED in 1 BOTTLE (71335-0822-9)
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A200629
ABAB
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": {
"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": "71335-0822_25e161db-5f02-4458-bec7-b5a99f425a19",
"productndc": "71335-0822",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "200629",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 250MG BASE",
"product_no": "001",
"approval_date": "Oct 31, 2011"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 500MG BASE",
"product_no": "002",
"approval_date": "Oct 31, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Naproxen Sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA200629",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20111031",
"active_numerator_strength": "550"
}Related drugs
Other records sharing ATC code G02CC02.
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