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United States · US · US:55910-500_0833bb77-1309-4ed7-ad4a-9b1044fb0799
dg health naproxen sodium
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDolgencorp Inc
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1155910500821 BOTTLE in 1 CARTON (55910-500-82) / 200 TABLET, FILM COATED in 1 BOTTLE
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": {
"5f0514bd-7893-4602-a17b-716fb9947572": {
"match": "brand_token",
"title": "DG HEALTH ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [DOLGENCORP INC]",
"spl_version": "9",
"published_date": "2026-02-10"
}
},
"productid": "55910-500_0833bb77-1309-4ed7-ad4a-9b1044fb0799",
"productndc": "55910-500",
"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": "dg health naproxen sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074661",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20131121",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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