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United States · US · US:55910-729_0c874a73-b144-40d7-bb3f-cb11f5cec8e5
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 · 3
- ndc1155910729621 BOTTLE in 1 CARTON (55910-729-62) / 24 TABLET, FILM COATED in 1 BOTTLE
- ndc1155910729711 BOTTLE in 1 CARTON (55910-729-71) / 50 TABLET, FILM COATED in 1 BOTTLE
- ndc1155910729751 BOTTLE in 1 CARTON (55910-729-75) / 90 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": "55910-729_0c874a73-b144-40d7-bb3f-cb11f5cec8e5",
"productndc": "55910-729",
"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": "20190612",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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