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United States · US · US:41163-707_726f2b53-4a2f-42db-8e7c-75da538df3fd
equaline naproxen sodium
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUnited Natural Foods, Inc. dba UNFI
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1141163707711 BOTTLE in 1 CARTON (41163-707-71) / 50 TABLET, FILM COATED in 1 BOTTLE
- ndc1141163707751 BOTTLE in 1 CARTON (41163-707-75) / 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": {
"8fc2389c-9657-4dbe-a32b-df8245fc67ca": {
"match": "brand_token",
"title": "EQUALINE DAYTIME AND NIGHTTIME COLD AND FLU RELIEF (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL) KIT [UNITED NATURAL FOODS, INC. DBA UNFI]",
"spl_version": "10",
"published_date": "2026-05-21"
}
},
"productid": "41163-707_726f2b53-4a2f-42db-8e7c-75da538df3fd",
"productndc": "41163-707",
"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": "equaline naproxen sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074661",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20140924",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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