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United States · US · US:63187-596_056f2617-2de4-4296-bd4d-714f34f7a15c
Naproxen Sodium
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc11631875962424 TABLET, FILM COATED in 1 BOTTLE (63187-596-24)
- ndc11631875962828 TABLET, FILM COATED in 1 BOTTLE (63187-596-28)
- ndc11631875963030 TABLET, FILM COATED in 1 BOTTLE (63187-596-30)
- ndc11631875966090 TABLET, FILM COATED in 1 BOTTLE (63187-596-60)
- ndc11631875969060 TABLET, FILM COATED in 1 BOTTLE (63187-596-90)
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A074661
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": "63187-596_056f2617-2de4-4296-bd4d-714f34f7a15c",
"productndc": "63187-596",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "074661",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Jan 13, 1997"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Naproxen Sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074661",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20140411",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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